Allele Registry

Canonical Allele Identifier: PA2826893649

Gene: FGD4 HGNC NCBI

ClinVar RCV:

RCV000168099

RCV000219132

RCV000857634

RCV001094112

RCV001174096

RCV002381537

RCV003982919

ClinVar Variation:

188187

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291412.1:p.Pro208Thr	CA334267 NM_001304483.2:c.622C>A