Canonical Allele Identifier: PA2825114401
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 964888
ClinVar RCV Id: RCV001239205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Val13Ala
CA398271725
NM_000304.4:c.38T>C