Canonical Allele Identifier: PA2826623439
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 431943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Leu78Pro
CA398268114
NM_001281455.2:c.233T>C