Canonical Allele Identifier: PA916019732
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308296
ClinVar RCV Id: RCV000654188 RCV001094111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291413.1:p.Leu56Val
CA6506846
NM_001304484.2:c.166C>G