Canonical Allele Identifier: PA2826623488
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662819
ClinVar RCV Id: RCV003441484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Ala113Thr
CA398739799
NM_001281455.2:c.337G>A