Allele Registry

Canonical Allele Identifier: PA2741921681

Gene: MYCN HGNC NCBI

ClinVar Allele:

3217415

ClinVar RCV:

RCV003964731

ClinVar Variation:

3058202

HGVS (amino-acid)	Matching Registered Transcripts
NP_005369.2:p.Pro44His	CA345930222 NM_005378.6:c.131C>A