Canonical Allele Identifier: PA916054982
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 586344
ClinVar RCV Id: RCV000712771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Leu11_Val13del
CA891843517
NM_153322.3:c.31_39del