Canonical Allele Identifier: PA249012
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292353.1:p.Pro951Leu
CA249011
NM_001305424.2:c.2852C>T