Allele Registry

Canonical Allele Identifier: PA112998

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015477

RCV000015478

ClinVar Variation:

14398

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Glu354Lys	CA123927 NM_000233.4:c.1060G>A