Allele Registry

Canonical Allele Identifier: PA658665632

Gene: CARD11 HGNC NCBI

ClinVar RCV:

RCV000528697

RCV000788795

RCV002285361

ClinVar Variation:

473938

HGVS (amino-acid)	Matching Registered Transcripts
NP_115791.3:p.Arg30Trp	CA366647967 NM_032415.6:c.88C>T