Canonical Allele Identifier: PA915995297
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 410321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Ala756Thr
CA2569799
NM_001178065.2:c.2266G>A