Canonical Allele Identifier: PA645483704
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 402493
ClinVar RCV Id: RCV000455928 RCV001643144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073594.1:p.Met1Thr