Canonical Allele Identifier: PA2829011995
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1165902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Val222Ile
CA6506686
NM_001385118.1:c.664G>A