Canonical Allele Identifier: PA2826623589
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ile24Met
CA398271663
NM_001281456.2:c.72C>G