Canonical Allele Identifier: PA2828405281
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507040
ClinVar RCV Id: RCV002009283 RCV004046196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Asp520Glu
CA6507120
NM_001370297.1:c.1560C>A
CA384372362
NM_001370297.1:c.1560C>G