Canonical Allele Identifier: PA2826831073
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_001280160.1:p.Arg187Trp
CA16042420
NM_001293231.2:c.559C>T