Canonical Allele Identifier: PA2825891354
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_001138881.1:p.Ala439dup
CA331037122
NM_001145409.2:c.1315_1317dup