Canonical Allele Identifier: PA1139721929
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 888217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002426.1:p.Asn273Ser
CA7662546
NM_002435.3:c.818A>G