Canonical Allele Identifier: PA112917
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 14388
ClinVar RCV Id: RCV000015466 RCV000015465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000224.2:p.Ala593Pro
CA123918
NM_000233.4:c.1777G>C