Canonical Allele Identifier: PA916055110
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 188095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gln103Arg
CA334032
NM_153322.3:c.308A>G