Canonical Allele Identifier: PA2825891409
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 450018
ClinVar RCV Id: RCV000522264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138882.1:p.Ala350dup
CA331037122
NM_001145410.1:c.1048_1050dup