Canonical Allele Identifier: PA2826623376
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 411592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Thr23Arg
CA16615515
NM_001281455.2:c.68C>G