Canonical Allele Identifier: PA2826281831
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 21728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.Tyr403Cys
CA342419
NM_001230.5:c.1208A>G