Allele Registry

Canonical Allele Identifier: PA2826379505

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV001327858

RCV004035260

ClinVar Variation:

1027284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Leu1108Arg	CA208225965 NM_001256267.2:c.3323T>G