Canonical Allele Identifier: PA2829312022
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 654340
ClinVar RCV Id: RCV000810280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387587.1:p.Arg245Gly
CA350294552
NM_001400658.1:c.733A>G