Canonical Allele Identifier: PA2828405531
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3026589
ClinVar RCV Id: RCV003886982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357227.2:p.Leu567Phe
CA384361156
NM_001370298.3:c.1699C>T