Canonical Allele Identifier: PA110446
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 411592
ClinVar RCV Id: RCV000518509 RCV000471834 RCV000789510 RCV001701010
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Thr23Arg
CA16615515
NM_000304.4:c.68C>G