Allele Registry

Canonical Allele Identifier: PA645489847

Gene: CARD11 HGNC NCBI

ClinVar RCV:

RCV000484392

RCV000499590

RCV003766695

ClinVar Variation:

421704

HGVS (amino-acid)	Matching Registered Transcripts
NP_115791.3:p.Arg975Trp	CA16618450 NM_032415.6:c.2923C>T