Canonical Allele Identifier: PA916055070
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 431943
ClinVar RCV Id: RCV000498886 RCV000518311 RCV000790161 RCV003581670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Leu78Pro
CA398268114
NM_153322.3:c.233T>C