Allele Registry

Canonical Allele Identifier: PA2826623766

Gene: PMP22 HGNC NCBI

ClinVar Variation Id: 637831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268385.1:p.Arg159Cys	CA8403293 NM_001281456.2:c.475C>T