Canonical Allele Identifier: PA2829011976
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 582380
ClinVar RCV Id: RCV000706433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Arg181Lys
CA6506653
NM_001385118.1:c.542G>A