Canonical Allele Identifier: PA2828933855
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371057.1:p.Met298Thr
CA339859
NM_001384128.1:c.893T>C