Canonical Allele Identifier: PA2826893900
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488316
ClinVar RCV Id: RCV001976975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291413.1:p.Tyr350Cys
CA6507112
NM_001304484.2:c.1049A>G