Allele Registry

Canonical Allele Identifier: PA645415316

Gene: MYCN HGNC NCBI

ClinVar Allele:

363339

ClinVar RCV:

RCV000421370

RCV000423772

RCV000428589

RCV000434477

RCV000441008

ClinVar Variation:

376460

HGVS (amino-acid)	Matching Registered Transcripts
NP_005369.2:p.Pro44Leu	CA16602894 NM_005378.6:c.131C>T