Canonical Allele Identifier: PA2826905043
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435213
ClinVar RCV Id: RCV000501423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001292353.1:p.Ser124Leu
CA345429179
NM_001305424.2:c.371C>T