Canonical Allele Identifier: PA2830276779
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 946236
ClinVar RCV Id: RCV001217059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_640334.2:p.Thr143Ala
CA384356230
NM_139241.3:c.427A>G