Canonical Allele Identifier: PA2573217432
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 402492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387594.1:p.Lys14Arg
CA2053387
NM_001400665.1:c.41A>G