Canonical Allele Identifier: PA645394363
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 433198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Gly150Val
CA398739500
NM_000304.4:c.449G>T