Canonical Allele Identifier: PA2826892644
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488316
ClinVar RCV Id: RCV001976975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Tyr779Cys
CA6507112
NM_001304481.1:c.2336A>G