Canonical Allele Identifier: PA645501996
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308284
ClinVar RCV Id: RCV000396677 RCV000439988 RCV001092390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Pro74Thr
CA6506547
NM_001304481.1:c.220C>A