Canonical Allele Identifier: PA645415361
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 372422
ClinVar RCV Id: RCV000414637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Arg398Trp
CA16042420
NM_005378.6:c.1192C>T