Canonical Allele Identifier: PA2828934455
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 245808
ClinVar RCV Id: RCV000236896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371060.1:p.Gly162Arg
CA6506640
NM_001384131.1:c.484G>C