Canonical Allele Identifier: PA2829313132
Gene: CASP8 HGNC NCBI
ClinVar RCV:
RCV000008201
ClinVar Variation:
7760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387593.1:p.Arg225Trp
CA119046
NM_001400664.1:c.673C>T