Allele Registry

Canonical Allele Identifier: PA112908

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015468

RCV002472931

ClinVar Variation:

14390

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Ala572Val	CA123920 NM_000233.4:c.1715C>T