Canonical Allele Identifier: PA915995295
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 463921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Ala756Val
CA2569800
NM_001178065.2:c.2267C>T