Canonical Allele Identifier: PA645415324
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 377368
ClinVar RCV Id: RCV000436958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Arg312Lys
CA1538282
NM_005378.6:c.935G>A