Allele Registry

Canonical Allele Identifier: PA2499242975

Gene: MYPN HGNC NCBI

ClinVar Allele:

1009119

ClinVar RCV:

RCV001324451

ClinVar Variation:

1024286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Val834Ile	CA376859183 NM_001256268.2:c.2500G>A