Canonical Allele Identifier: PA2828405137
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Leu216Val
CA6506846
NM_001370297.1:c.646C>G