Allele Registry

Canonical Allele Identifier: PA112960

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015475

ClinVar Variation:

14396

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Cys131Arg	CA123925 NM_000233.4:c.391T>C