Canonical Allele Identifier: PA2826893703
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 623800
ClinVar RCV Id: RCV000761820 RCV002397533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291412.1:p.Ala326Val
CA384367854
NM_001304483.2:c.977C>T