Canonical Allele Identifier: PA645294220
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 382636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ala135Thr
CA8403306
NM_000304.4:c.403G>A