Canonical Allele Identifier: PA1139694819
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 950661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Gln1038Arg
CA354161401
NM_001178065.2:c.3113A>G