Canonical Allele Identifier: PA2827307832
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1012006
ClinVar RCV Id: RCV001309895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Cys9Tyr
CA384355973
NM_001330373.1:c.26G>A