Canonical Allele Identifier: PA2829011934
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 954240
ClinVar RCV Id: RCV001226665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Ala108Thr
CA384356014
NM_001385118.1:c.322G>A