Allele Registry

Canonical Allele Identifier: PA2826150499

Gene: CARD8 HGNC NCBI

ClinVar RCV:

RCV001484252

RCV003938867

ClinVar Variation:

1145399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171831.1:p.Pro386Leu	CA9547786 NM_001184902.2:c.1157C>T