Canonical Allele Identifier: PA2829012009
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 849450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Ser244Leu
CA6506711
NM_001385118.1:c.731C>T