Canonical Allele Identifier: PA116395
Gene: MPO HGNC NCBI

Linked Data

ClinVar Variation Id: 3634
ClinVar RCV Id: RCV000003819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000241.1:p.Gly501Ser
CA116393
NM_000250.2:c.1501G>A