Allele Registry

Canonical Allele Identifier: PA916009253

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV000622040

RCV001218437

RCV001566793

ClinVar Variation:

520383

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Pro808Leu	CA5523018 NM_001256268.2:c.2423C>T