Canonical Allele Identifier: PA110188
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8443
ClinVar RCV Id: RCV000008956 RCV001173915 RCV002288476 RCV003581556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ala67Thr
CA254388
NM_000304.4:c.199G>A