Canonical Allele Identifier: PA2826892514
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141629
ClinVar RCV Id: RCV003074001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Glu498Asp
CA384361044
NM_001304481.1:c.1494A>C
CA384361045
NM_001304481.1:c.1494A>T