Canonical Allele Identifier: PA2829317047
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476396
ClinVar RCV Id: RCV001977929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387679.1:p.Val26Leu
CA350293648
NM_001400750.1:c.76G>C