Canonical Allele Identifier: PA2827428792
Gene: FMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435213
ClinVar RCV Id: RCV000501423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335023.1:p.Ser124Leu
CA345429179
NM_001348094.2:c.371C>T