Canonical Allele Identifier: PA2829317052
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301833
ClinVar RCV Id: RCV002886729 RCV003619814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387679.1:p.Cys37Arg
CA350294001
NM_001400750.1:c.109T>C