Canonical Allele Identifier: PA2826283890
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715731
ClinVar RCV Id: RCV002301466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Ile392Ser
CA63866548
NM_001206524.2:c.1175T>G