Allele Registry

Canonical Allele Identifier: PA2580180381

Gene: MYPN HGNC NCBI

ClinVar Allele:

2019721

ClinVar RCV:

RCV002710339

ClinVar Variation:

1959587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Pro807Ser	CA376858907 NM_001256268.2:c.2419C>T