Canonical Allele Identifier: PA2826623359
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 586344
ClinVar RCV Id: RCV000712771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Leu11_Val13del
CA891843517
NM_001281455.2:c.31_39del