Canonical Allele Identifier: PA2826892457
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291410.1:p.Met383Thr
CA339859
NM_001304481.1:c.1148T>C