Canonical Allele Identifier: PA915995079
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 432667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Glu568Gly
CA354156245
NM_001178065.2:c.1703A>G