Canonical Allele Identifier: PA2826892393
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 245601
ClinVar RCV Id: RCV000236369 RCV001173484 RCV001079406 RCV001114309 RCV002338766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Gly245Asp
CA6506638
NM_001304481.1:c.734G>A