Canonical Allele Identifier: PA645471417
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 423531
ClinVar RCV Id: RCV000484363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Trp491Arg
CA16617732
NM_000233.4:c.1471T>C
CA346746813
NM_000233.4:c.1471T>A