Canonical Allele Identifier: PA915994711
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 60667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Pro221Leu
CA144609
NM_001178065.2:c.662C>T