Canonical Allele Identifier: PA2826623500
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 586345
ClinVar RCV Id: RCV000712772 RCV000844937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.His121Arg
CA398739730
NM_001281455.2:c.362A>G