Canonical Allele Identifier: PA916055196
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637387
ClinVar RCV Id: RCV000789530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Arg157Gly
CA398739445
NM_153322.3:c.469C>G