Canonical Allele Identifier: PA916055191
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly150Cys
CA119624
NM_153322.3:c.448G>T