Canonical Allele Identifier: PA658808067
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 523483
ClinVar RCV Id: RCV000626880 RCV001662671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Pro409Leu
CA345932549
NM_005378.6:c.1226C>T