Canonical Allele Identifier: PA2826623580
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1751590
ClinVar RCV Id: RCV002360138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Phe20Leu
CA398271684
NM_001281456.2:c.60C>G
CA398271685
NM_001281456.2:c.60C>A
CA398271691
NM_001281456.2:c.58T>C