Canonical Allele Identifier: PA2580189374
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2279877
ClinVar RCV Id: RCV002813984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Ala95Thr
CA1538276
NM_001293231.2:c.283G>A