Allele Registry

Canonical Allele Identifier: PA112986

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015464

ClinVar Variation:

14387

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Cys543Arg	CA250646 NM_000233.4:c.1627T>C