Canonical Allele Identifier: PA891845578
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 570254
ClinVar RCV Id: RCV000691075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Arg159His
CA288864488
NM_000304.4:c.476G>A