Allele Registry

Canonical Allele Identifier: PA2826623397

Gene: PMP22 HGNC NCBI

ClinVar Allele:

23481

ClinVar RCV:

RCV000008955

ClinVar Variation:

8442

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268384.1:p.Asp37Val	CA119626 NM_001281455.2:c.110A>T