Canonical Allele Identifier: PA2829311664
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533732
ClinVar RCV Id: RCV000640975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387585.1:p.Ile298Val
CA2053716
NM_001400656.1:c.892A>G