Canonical Allele Identifier: PA2826831046
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2808432
ClinVar RCV Id: RCV003684849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Val128Leu
CA1538297
NM_001293231.2:c.382G>T
CA345932089
NM_001293231.2:c.382G>C