Canonical Allele Identifier: PA2828934559
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543399
ClinVar RCV Id: RCV000654153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371061.1:p.Ser146Ile
CA384356252
NM_001384132.1:c.437G>T