Allele Registry

Canonical Allele Identifier: PA358279

Gene: MYPN HGNC NCBI

ClinVar Allele:

40479

ClinVar RCV:

RCV000024512

RCV000206974

RCV000216191

RCV000247848

RCV000624690

RCV000852614

ClinVar Variation:

31819

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Leu1161Ile	CA215338 NM_001256267.2:c.3481C>A