Canonical Allele Identifier: PA2827307839
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 859067
ClinVar RCV Id: RCV001065093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317302.1:p.Lys13Glu
CA384356002
NM_001330373.1:c.37A>G