Canonical Allele Identifier: PA2828405516
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_001357227.2:p.Glu535Asp
CA384360938
NM_001370298.3:c.1605G>C
CA384360939
NM_001370298.3:c.1605G>T