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Title: NM_000233.3(LHCGR):c.1847C>A (p.Ser616Tyr) AND Leydig hypoplasia, type I  
type:
Variation
ID:
9606
species:
human
accesstypes:
download
authorization:
none
authentication:
none
dateModified:
10-05-2016
ID:
35737
dateSubmitted:
06-20-2011
ID:
SCV000035737
ID:
152790.0009
title:
LHCGR, SER616TYR_LEYDIG HYPOPLASIA, TYPE I
name:
National Center for Biotechnology Information
abbreviation:
NCBI
homePage: https://www.ncbi.nlm.nih.gov/
name:
ClinVar
abbreviation:
ClinVar
homePage: https://www.ncbi.nlm.nih.gov/clinvar/

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