Allele Registry

Canonical Allele Identifier: PA658818405

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV000622040

RCV001218437

RCV001566793

ClinVar Variation:

520383

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Pro1102Leu	CA5523018 NM_032578.4:c.3305C>T