Allele Registry

Canonical Allele Identifier: PA2826623680

Gene: PMP22 HGNC NCBI

ClinVar RCV:

RCV000167942

RCV000493971

ClinVar Variation:

188095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268385.1:p.Gln103Arg	CA334032 NM_001281456.2:c.308A>G