Canonical Allele Identifier: PA2826623635
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 531685
ClinVar RCV Id: RCV000638164 RCV001731826 RCV002420718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Met69Thr
CA288098399
NM_001281456.2:c.206T>C