Canonical Allele Identifier: PA2829313299
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387594.1:p.Asp260His
CA119051
NM_001400665.1:c.778G>C