Canonical Allele Identifier: PA916055174
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637381
ClinVar RCV Id: RCV000789523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Leu147Arg
CA398739522
NM_153322.3:c.440T>G