Canonical Allele Identifier: PA119049
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7760
ClinVar RCV Id: RCV000008201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001219.2:p.Arg265Trp
CA119046
NM_001228.4:c.793C>T