Canonical Allele Identifier: PA2826893831
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 662801
ClinVar RCV Id: RCV000820538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291413.1:p.Met220Ile
CA384367593
NM_001304484.2:c.660G>A
CA384367596
NM_001304484.2:c.660G>C
CA384367599
NM_001304484.2:c.660G>T