Canonical Allele Identifier: PA2829011928
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 863466
ClinVar RCV Id: RCV001070436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Gln99His
CA235437798
NM_001385118.1:c.297G>T
CA384355952
NM_001385118.1:c.297G>C