Canonical Allele Identifier: PA2825114607
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908552
ClinVar RCV Id: RCV003740898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Leu138Pro
CA398739596
NM_000304.4:c.413T>C