Canonical Allele Identifier: PA2830108871
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715731
ClinVar RCV Id: RCV002301466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Ile459Ser
CA63866548
NM_032974.5:c.1376T>G