Canonical Allele Identifier: PA2826623685
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 694892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ala106Asp
CA398267382
NM_001281456.2:c.317C>A