Canonical Allele Identifier: PA2826623465
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2095123
ClinVar RCV Id: RCV003012182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Thr99Ile
CA398267441
NM_001281455.2:c.296C>T