Canonical Allele Identifier: PA2829011998
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137246
ClinVar RCV Id: RCV003058352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372047.1:p.Asn223Thr
CA235204118
NM_001385118.1:c.668A>C