Canonical Allele Identifier: PA2826831000
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 433153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280157.1:p.Arg394Leu
CA345932452
NM_001293228.1:c.1181G>T