Canonical Allele Identifier: PA916055105
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637375
ClinVar RCV Id: RCV000789516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly100Glu
CA398267432
NM_153322.3:c.299G>A