Allele Registry

Canonical Allele Identifier: PA2829313157

Gene: CASP8 HGNC NCBI

ClinVar RCV:

RCV000640975

ClinVar Variation:

533732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001387593.1:p.Ile275Val	CA2053716 NM_001400664.1:c.823A>G