Canonical Allele Identifier: PA2829310617
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577
ClinVar RCV Id: RCV001048674 RCV001772251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387577.1:p.Asp259Asn
CA2053660
NM_001400648.1:c.775G>A