Canonical Allele Identifier: PA2829314496
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387603.1:p.Asp54Asn
CA2053660
NM_001400674.1:c.160G>A