Allele Registry

Canonical Allele Identifier: PA2826379500

Gene: MYPN HGNC NCBI

ClinVar Allele:

1493008

ClinVar RCV:

RCV001881215

ClinVar Variation:

1378578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Pro1101Leu	CA376858915 NM_001256267.2:c.3302C>T