Allele Registry

Canonical Allele Identifier: PA2826380300

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV004519880

ClinVar Variation:

3228170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Gln844Leu	CA376859272 NM_001256268.2:c.2531A>T