Canonical Allele Identifier: PA2829310038
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 402492
ClinVar RCV Id: RCV000455301 RCV001675894 RCV001518111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387571.1:p.Lys14Arg
CA2053387
NM_001400642.1:c.41A>G