Canonical Allele Identifier: PA2826623367
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Leu16Pro
CA340784
NM_001281455.2:c.47T>C