Canonical Allele Identifier: PA658805031
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 531685
ClinVar RCV Id: RCV000638164 RCV001731826 RCV002420718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Met69Thr
CA288098399
NM_000304.4:c.206T>C