Allele Registry

Canonical Allele Identifier: PA916055196

Gene: PMP22 HGNC NCBI

ClinVar RCV:

RCV000789530

ClinVar Variation:

637387

HGVS (amino-acid)	Matching Registered Transcripts
NP_696997.1:p.Arg157Gly	CA398739445 NM_153322.3:c.469C>G