Canonical Allele Identifier: PA658660094
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 448092
ClinVar RCV Id: RCV000516704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Pro144Arg
CA398739549
NM_000304.4:c.431C>G