Canonical Allele Identifier: PA2827328651
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637373
ClinVar RCV Id: RCV000789514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317072.1:p.Leu18Arg
CA398271697
NM_001330143.2:c.53T>G