Canonical Allele Identifier: PA113101
Gene: LHCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 14389

Amino-acid Alleles

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