Canonical Allele Identifier: PA2580465687
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715731
ClinVar RCV Id: RCV002301466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Ile459Ser
CA63866548
NM_032977.3:c.1376T>G