Canonical Allele Identifier: PA2825464610
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073593.1:p.Asp244Asn
CA2053660
NM_001080124.1:c.730G>A