Canonical Allele Identifier: PA2826762575
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 585033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276085.1:p.Ser22Arg
CA7662393
NM_001289156.2:c.64A>C
CA393171285
NM_001289156.2:c.66C>A
CA393171289
NM_001289156.2:c.66C>G