Canonical Allele Identifier: PA645441992
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377373
ClinVar RCV Id: RCV000430664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292353.1:p.Ala260Thr
CA1476236
NM_001305424.2:c.778G>A