Canonical Allele Identifier: PA2827328667
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349839
ClinVar RCV Id: RCV002039305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317072.1:p.Thr23Lys
CA288109904
NM_001330143.2:c.68C>A