Canonical Allele Identifier: PA915995632
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 641351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Val1081Ile
CA354161788
NM_001178065.2:c.3241G>A