Canonical Allele Identifier: PA2826623406
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 215728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.His51Arg
CA337251
NM_001281455.2:c.152A>G