Canonical Allele Identifier: PA2830106285
Gene: CASP8 HGNC NCBI
ClinVar RCV:
RCV000640975
ClinVar Variation:
533732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203519.1:p.Ile298Val
CA2053716
NM_033355.3:c.892A>G