Canonical Allele Identifier: PA248904
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218767
ClinVar RCV Id: RCV000202705 RCV003417736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292353.1:p.Ala1142Val
CA248903
NM_001305424.2:c.3425C>T