Canonical Allele Identifier: PA916055116
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly107Val
CA398739843
NM_153322.3:c.320G>T