Allele Registry

Canonical Allele Identifier: PA2499242974

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV001327858

RCV004035260

ClinVar Variation:

1027284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.Leu814Arg	CA208225965 NM_001256268.2:c.2441T>G