Canonical Allele Identifier: PA2828405133
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 948484
ClinVar RCV Id: RCV001219747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Glu214Asp
CA384360938
NM_001370297.1:c.642G>C
CA384360939
NM_001370297.1:c.642G>T