Canonical Allele Identifier: PA110419
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ser79Cys
CA254385
NM_000304.4:c.236C>G