Canonical Allele Identifier: PA2826623381
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 889626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Val25Gly
CA8403451
NM_001281455.2:c.74T>G