Canonical Allele Identifier: PA2829604443
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_005369.2:p.Thr300Ile
CA16040252
NM_005378.6:c.899C>T