Canonical Allele Identifier: PA2826830979
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_001280157.1:p.Val339Leu
CA1538297
NM_001293228.1:c.1015G>T
CA345932089
NM_001293228.1:c.1015G>C