Allele Registry

Canonical Allele Identifier: PA2573164709

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV001949425

ClinVar Variation:

1458111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Asp564Val	CA346745190 NM_000233.4:c.1691A>T