Canonical Allele Identifier: PA2580189372
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1955185
ClinVar RCV Id: RCV002715221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Thr89Ile
CA16040252
NM_001293231.2:c.266C>T