Canonical Allele Identifier: PA2827307930
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1165902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Val129Ile
CA6506686
NM_001330373.1:c.385G>A