Canonical Allele Identifier: PA2742018472
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662819
ClinVar RCV Id: RCV003441484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Ala113Thr
CA398739799
NM_153322.3:c.337G>A