Canonical Allele Identifier: PA2826892356
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 863466
ClinVar RCV Id: RCV001070436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Gln184His
CA235437798
NM_001304481.1:c.552G>T
CA384355952
NM_001304481.1:c.552G>C