Canonical Allele Identifier: PA2826623749
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2913861
ClinVar RCV Id: RCV003740999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Leu147Pro
CA398739523
NM_001281456.2:c.440T>C