Allele Registry

Canonical Allele Identifier: PA2826379527

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV004519880

ClinVar Variation:

3228170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Gln1138Leu	CA376859272 NM_001256267.2:c.3413A>T