Canonical Allele Identifier: PA2829313135
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 639795
ClinVar RCV Id: RCV000792694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387593.1:p.Leu231Arg
CA350294407
NM_001400664.1:c.692T>G