Canonical Allele Identifier: PA2826892513
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 566730
ClinVar RCV Id: RCV000686620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Glu499del
CA604224658
NM_001304481.1:c.1497_1499del