Canonical Allele Identifier: PA2829011978
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 938113
ClinVar RCV Id: RCV001207267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Asn183Asp
CA384356488
NM_001385118.1:c.547A>G