Allele Registry

Canonical Allele Identifier: PA113081

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015462

RCV001886947

ClinVar Variation:

14385

1389006

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Met571Ile	CA123917 NM_000233.4:c.1713G>A CA346745029 NM_000233.4:c.1713G>T CA346745030 NM_000233.4:c.1713G>C