Canonical Allele Identifier: PA2829012075
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 948484
ClinVar RCV Id: RCV001219747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Glu398Asp
CA384360938
NM_001385118.1:c.1194G>C
CA384360939
NM_001385118.1:c.1194G>T