Canonical Allele Identifier: PA915995393
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 381654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Met821Val
CA16604354
NM_001178065.2:c.2461A>G