Allele Registry

Canonical Allele Identifier: PA185999

Gene: CARD11 HGNC NCBI

ClinVar RCV:

RCV000162028

RCV001850281

ClinVar Variation:

183144

HGVS (amino-acid)	Matching Registered Transcripts
NP_115791.3:p.Gly123Asp	CA185998 NM_032415.6:c.368G>A