Canonical Allele Identifier: PA2826892508
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Leu485Val
CA6506846
NM_001304481.1:c.1453C>G