Canonical Allele Identifier: PA2826623634
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637834
ClinVar RCV Id: RCV000790164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Met69Arg
CA398268285
NM_001281456.2:c.206T>G