Canonical Allele Identifier: PA2825114532
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 2095123
ClinVar RCV Id: RCV003012182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Thr99Ile
CA398267441
NM_000304.4:c.296C>T