Allele Registry

Canonical Allele Identifier: PA2826150697

Gene: CARD8 HGNC NCBI

ClinVar RCV:

RCV003778645

RCV004245335

ClinVar Variation:

2409418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171832.1:p.Phe354Leu	CA9547804 NM_001184903.1:c.1062C>G CA406665356 NM_001184903.1:c.1062C>A CA406665360 NM_001184903.1:c.1060T>C