Canonical Allele Identifier: PA2825153525
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 532619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Phe862Ser
CA2569836
NM_000388.4:c.2585T>C