Allele Registry

Canonical Allele Identifier: PA916055048

Gene: PMP22 HGNC NCBI

ClinVar RCV:

RCV000790164

ClinVar Variation:

637834

HGVS (amino-acid)	Matching Registered Transcripts
NP_696997.1:p.Met69Arg	CA398268285 NM_153322.3:c.206T>G