Canonical Allele Identifier: PA2826762437
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 585033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276084.1:p.Ser72Arg
CA7662393
NM_001289155.2:c.214A>C
CA393171285
NM_001289155.2:c.216C>A
CA393171289
NM_001289155.2:c.216C>G