Canonical Allele Identifier: PA915995390
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 379931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Asn812Ser
CA2569822
NM_001178065.2:c.2435A>G