Allele Registry

Canonical Allele Identifier: PA2826150069

Gene: CARD8 HGNC NCBI

ClinVar RCV:

RCV001514794

ClinVar Variation:

1166485

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171830.1:p.Phe52Ile	CA9548101 NM_001184901.1:c.154T>A