Canonical Allele Identifier: PA2827308590
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 566730
ClinVar RCV Id: RCV000686620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Glu321del
CA604224658
NM_001330374.1:c.963_965del