Canonical Allele Identifier: PA2826892650
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056618
ClinVar RCV Id: RCV001365479 RCV004036943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Ala788Thr
CA6507118
NM_001304481.1:c.2362G>A