Allele Registry

Canonical Allele Identifier: PA113053

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015489

ClinVar Variation:

14408

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Leu457Arg	CA123934 NM_000233.4:c.1370T>G