Allele Registry

Canonical Allele Identifier: PA2830086765

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV001324451

ClinVar Variation:

1024286

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Val1128Ile	CA376859183 NM_032578.4:c.3382G>A