Canonical Allele Identifier: PA2828405368
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 863466
ClinVar RCV Id: RCV001070436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357227.2:p.Gln236His
CA235437798
NM_001370298.3:c.708G>T
CA384355952
NM_001370298.3:c.708G>C