This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2825114555
Gene: PMP22 HGNC NCBI
ClinVar RCV:
RCV003441484
ClinVar Variation:
2662819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ala113Thr
CA398739799
NM_000304.4:c.337G>A