Canonical Allele Identifier: PA2829012216
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488316
ClinVar RCV Id: RCV001976975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Tyr694Cys
CA6507112
NM_001385118.1:c.2081A>G