Canonical Allele Identifier: PA916055077
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 217236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Ser79Thr
CA279110
NM_153322.3:c.235T>A