Canonical Allele Identifier: PA2826623665
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 888946
ClinVar RCV Id: RCV001122568 RCV001122569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Thr89Asn
CA288098306
NM_001281456.2:c.266C>A