Canonical Allele Identifier: PA2826623397
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8442
ClinVar RCV Id: RCV000008955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Asp37Val
CA119626
NM_001281455.2:c.110A>T