Canonical Allele Identifier: PA2499254553
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015705
ClinVar RCV Id: RCV001314607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357226.1:p.Arg35Thr
CA384357148
NM_001370297.1:c.104G>C