Canonical Allele Identifier: PA915994932
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 64427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Asp398Asn
CA216118
NM_001178065.2:c.1192G>A