Canonical Allele Identifier: PA2826623573
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1687565
ClinVar RCV Id: RCV002251247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.His12Tyr
CA398271733
NM_001281456.2:c.34C>T