Canonical Allele Identifier: PA2829310375
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387574.1:p.Asp270Asn
CA2053660
NM_001400645.1:c.808G>A