Canonical Allele Identifier: PA2826623358
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035915
ClinVar RCV Id: RCV001338852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Ile9Val
CA8403455
NM_001281455.2:c.25A>G