Allele Registry

Canonical Allele Identifier: PA2826623763

Gene: PMP22 HGNC NCBI

ClinVar RCV:

RCV000789530

ClinVar Variation:

637387

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268385.1:p.Arg157Gly	CA398739445 NM_001281456.2:c.469C>G