Canonical Allele Identifier: PA2829311062
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051083
ClinVar RCV Id: RCV001359074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387582.1:p.Asp223Asn
CA2053646
NM_001400653.1:c.667G>A