Canonical Allele Identifier: PA2826831008
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_001280157.1:p.Pro409Leu
CA345932549
NM_001293228.1:c.1226C>T