Canonical Allele Identifier: PA2826284198
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715731
ClinVar RCV Id: RCV002301466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Ile416Ser
CA63866548
NM_001206542.2:c.1247T>G