Canonical Allele Identifier: PA346828
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188373
ClinVar RCV Id: RCV000236955 RCV000727143 RCV001080120 RCV001114409 RCV002426801 RCV003937521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_640334.2:p.Val717Met
CA346827
NM_139241.3:c.2149G>A