Canonical Allele Identifier: PA2826623763
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637387
ClinVar RCV Id: RCV000789530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Arg157Gly
CA398739445
NM_001281456.2:c.469C>G