Canonical Allele Identifier: PA645415358
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 433153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Arg394Leu
CA345932452
NM_005378.6:c.1181G>T