Canonical Allele Identifier: PA110320
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637819
ClinVar RCV Id: RCV000790143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Leu71Pro
CA398268247
NM_000304.4:c.212T>C