Allele Registry

Canonical Allele Identifier: PA2826892457

Gene: FGD4 HGNC NCBI

ClinVar RCV:

RCV000001070

RCV000789103

ClinVar Variation:

1015

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291410.1:p.Met383Thr	CA339859 NM_001304481.1:c.1148T>C