Canonical Allele Identifier: PA645294214
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 235779
ClinVar RCV Id: RCV000224582 RCV001050263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Leu82Pro
CA10581428
NM_000304.4:c.245T>C