Canonical Allele Identifier: PA2825114616
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2111792
ClinVar RCV Id: RCV003046166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Val141Met
CA288864491
NM_000304.4:c.421G>A