Canonical Allele Identifier: PA916055104
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637820
ClinVar RCV Id: RCV000790144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly100Arg
CA398267436
NM_153322.3:c.298G>A
CA398267437
NM_153322.3:c.298G>C