Canonical Allele Identifier: PA2829315221
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387609.1:p.Asp80His
CA119051
NM_001400680.1:c.238G>C