Canonical Allele Identifier: PA2827308597
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 245919
ClinVar RCV Id: RCV000236012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Glu333Asp
CA10584432
NM_001330374.1:c.999A>C
CA384361133
NM_001330374.1:c.999A>T