Allele Registry

Canonical Allele Identifier: PA645471417

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000484363

ClinVar Variation:

423531

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Trp491Arg	CA16617732 NM_000233.4:c.1471T>C CA346746813 NM_000233.4:c.1471T>A