Canonical Allele Identifier: PA2829317165
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7762
ClinVar RCV Id: RCV000008203 RCV000454902 RCV000308703 RCV001711066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387680.1:p.Asp71His
CA119051
NM_001400751.1:c.211G>C