Canonical Allele Identifier: PA2829012102
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188187
ClinVar RCV Id: RCV000168099 RCV000219132 RCV000857634 RCV001174096 RCV001094112 RCV002381537 RCV003982919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Pro456Thr
CA334267
NM_001385118.1:c.1366C>A