Canonical Allele Identifier: PA916055150
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 382636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Ala135Thr
CA8403306
NM_153322.3:c.403G>A