Allele Registry

Canonical Allele Identifier: PA2573189491

Gene: MYPN HGNC NCBI

ClinVar Allele:

1493008

ClinVar RCV:

RCV001881215

ClinVar Variation:

1378578

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Pro807Leu	CA376858915 NM_001256268.2:c.2420C>T