Canonical Allele Identifier: PA2825114634
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 917226
ClinVar RCV Id: RCV001173919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Leu156Ser
CA398739450
NM_000304.4:c.467T>C