Canonical Allele Identifier: PA2828405597
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 623800
ClinVar RCV Id: RCV000761820 RCV002397533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357227.2:p.Ala711Val
CA384367854
NM_001370298.3:c.2132C>T