Canonical Allele Identifier: PA2829311664
Gene: CASP8 HGNC NCBI
ClinVar RCV:
RCV000640975
ClinVar Variation:
533732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387585.1:p.Ile298Val
CA2053716
NM_001400656.1:c.892A>G