Allele Registry

Canonical Allele Identifier: PA2826379499

Gene: MYPN HGNC NCBI

ClinVar Allele:

1792204

ClinVar RCV:

RCV002454707

ClinVar Variation:

1729997

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Pro1101His	CA376858908 NM_001256267.2:c.3302C>A