Canonical Allele Identifier: PA2829012029
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015
ClinVar RCV Id: RCV000001070 RCV000789103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Met298Thr
CA339859
NM_001385118.1:c.893T>C