Allele Registry

Canonical Allele Identifier: PA2826379461

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV000621402

RCV000861131

RCV001293105

ClinVar Variation:

518889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Ser1056Phe	CA5522980 NM_001256267.2:c.3167C>T