Canonical Allele Identifier: PA110214
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637820
ClinVar RCV Id: RCV000790144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Gly100Arg
CA398267436
NM_000304.4:c.298G>A
CA398267437
NM_000304.4:c.298G>C