Canonical Allele Identifier: PA2829313152
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387593.1:p.Asp262His
CA119051
NM_001400664.1:c.784G>C