Canonical Allele Identifier: PA2829314767
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387605.1:p.Asp71His
CA119051
NM_001400676.1:c.211G>C