Canonical Allele Identifier: PA257010
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 13892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Arg393His
CA257009
NM_005378.6:c.1178G>A