Allele Registry

Canonical Allele Identifier: PA113101

Gene: LHCGR HGNC NCBI

ClinVar RCV:

RCV000015467

RCV002466405

ClinVar Variation:

14389

HGVS (amino-acid)	Matching Registered Transcripts
NP_000224.2:p.Thr577Ile	CA123919 NM_000233.4:c.1730C>T