Canonical Allele Identifier: PA916055038
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 188195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Leu62Arg
CA334283
NM_153322.3:c.185T>G