Canonical Allele Identifier: PA1139696944
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 839901
ClinVar RCV Id: RCV001041763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317303.1:p.Glu98Asp
CA384356543
NM_001330374.1:c.294G>C
CA384356544
NM_001330374.1:c.294G>T