Canonical Allele Identifier: PA915995437
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 532619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Phe872Ser
CA2569836
NM_001178065.2:c.2615T>C