Canonical Allele Identifier: PA2580251787
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2037856
ClinVar RCV Id: RCV002890277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387608.1:p.Pro205Leu
CA350293696
NM_001400679.1:c.614C>T