Allele Registry

Canonical Allele Identifier: PA2830086733

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV001327858

RCV004035260

ClinVar Variation:

1027284

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Leu1108Arg	CA208225965 NM_032578.4:c.3323T>G