Canonical Allele Identifier: PA2828933394
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 859067
ClinVar RCV Id: RCV001065093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371056.1:p.Lys106Glu
CA384356002
NM_001384127.1:c.316A>G