Canonical Allele Identifier: PA2829313456
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387595.1:p.Asp216His
CA119051
NM_001400666.1:c.646G>C