Canonical Allele Identifier: PA2829310366
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387574.1:p.Gly245Glu
CA350293942
NM_001400645.1:c.734G>A