Canonical Allele Identifier: PA1139748383
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 994920
ClinVar RCV Id: RCV001288682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly133Asp
CA398739636
NM_153322.3:c.398G>A