Canonical Allele Identifier: PA2828405068
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543490
ClinVar RCV Id: RCV000654264 RCV001114310 RCV002360663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Asn28Ser
CA6506682
NM_001370297.1:c.83A>G