Canonical Allele Identifier: PA915995209
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 35786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Pro682Thr
CA213577
NM_001178065.2:c.2044C>A