Canonical Allele Identifier: PA645442136
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435231
ClinVar RCV Id: RCV000499429 RCV000899884 RCV001264630 RCV001336476 RCV002527252 RCV003935288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292353.1:p.Ser1544Leu
CA1477572
NM_001305424.2:c.4631C>T