Canonical Allele Identifier: PA113291
Gene: NOL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 39803
ClinVar RCV Id: RCV000033024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263236.1:p.Glu21Gln
CA130568
NM_001276307.3:c.61G>C