Canonical Allele Identifier: PA915994931
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 420106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Gly397Arg
CA16617817
NM_001178065.2:c.1189G>A
CA354152779
NM_001178065.2:c.1189G>C