Canonical Allele Identifier: PA2826892406
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 938113
ClinVar RCV Id: RCV001207267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Asn268Asp
CA384356488
NM_001304481.1:c.802A>G