Canonical Allele Identifier: PA2580189369
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2105662
ClinVar RCV Id: RCV003014978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Asp54Val
CA345931615
NM_001293231.2:c.161A>T