Canonical Allele Identifier: PA2826893700
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058641
ClinVar RCV Id: RCV001367802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291412.1:p.Pro323Leu
CA6506990
NM_001304483.2:c.968C>T