Allele Registry

Canonical Allele Identifier: PA203897

Gene: CARD11 HGNC NCBI

ClinVar Allele:

199872

ClinVar RCV:

RCV000185616

RCV001390618

ClinVar Variation:

203461

HGVS (amino-acid)	Matching Registered Transcripts
NP_115791.3:p.Cys49Tyr	CA203896 NM_032415.6:c.146G>A