Canonical Allele Identifier: PA2830106479
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203520.1:p.Asp244Asn
CA2053660
NM_033356.4:c.730G>A