Allele Registry

Canonical Allele Identifier: PA113092

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015472

RCV002514103

RCV003137526

ClinVar Variation:

14393

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Ser616Tyr	CA123923 NM_000233.4:c.1847C>A