Canonical Allele Identifier: PA2580538033
Gene: FGD2 HGNC NCBI
ClinVar RCV:
RCV004224745
ClinVar Variation:
2387880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775829.2:p.Asp418Glu
CA3783221
NM_173558.4:c.1254C>A
CA363860698
NM_173558.4:c.1254C>G