Canonical Allele Identifier: PA354554
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064450.3:p.Ala1138Val
CA248903
NM_020066.4:c.3413C>T