Canonical Allele Identifier: PA1139721885
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 989847
ClinVar RCV Id: RCV001277748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002426.1:p.Gly247Ser
CA7662532
NM_002435.3:c.739G>A