Canonical Allele Identifier: PA2830323029
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696996.1:p.Trp28Arg
CA342724
NM_153321.3:c.82T>C
CA398271198
NM_153321.3:c.82T>A