Allele Registry

Canonical Allele Identifier: PA112944

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015461

RCV000517056

RCV000583503

RCV000763499

ClinVar Variation:

14384

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Asp578Gly	CA123916 NM_000233.4:c.1733A>G