Canonical Allele Identifier: PA915967805
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533732
ClinVar RCV Id: RCV000640975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073594.1:p.Ile357Val
CA2053716
NM_001080125.1:c.1069A>G