Allele Registry

This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.

Canonical Allele Identifier: PA2826379529

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV002452188

RCV003102372

RCV003319518

ClinVar Variation:

1731203

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Arg1139Cys	CA5523036 NM_001256267.2:c.3415C>T