Canonical Allele Identifier: PA915994851
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 342798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Lys336Asn
CA2569572
NM_001178065.2:c.1008G>T
CA2569573
NM_001178065.2:c.1008G>C