Canonical Allele Identifier: PA2826623731
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 382636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ala135Thr
CA8403306
NM_001281456.2:c.403G>A