Canonical Allele Identifier: PA2573294047
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Ala259Val
CA2053045
NM_032977.3:c.776C>T