Canonical Allele Identifier: PA2826893637
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 245919
ClinVar RCV Id: RCV000236012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291412.1:p.Glu178Asp
CA10584432
NM_001304483.2:c.534A>C
CA384361133
NM_001304483.2:c.534A>T