Canonical Allele Identifier: PA915995313
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 35790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Arg762Cys
CA213584
NM_001178065.2:c.2284C>T