Allele Registry

Canonical Allele Identifier: PA116392

Gene: MPO HGNC NCBI

ClinVar Allele:

18670

ClinVar RCV:

RCV000003815

ClinVar Variation:

3631

HGVS (amino-acid)	Matching Registered Transcripts
NP_000241.1:p.Leu572Trp	CA116390 NM_000250.2:c.1715T>G