Canonical Allele Identifier: PA2826623631
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ala67Thr
CA254388
NM_001281456.2:c.199G>A