Canonical Allele Identifier: PA2826623695
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637370
ClinVar RCV Id: RCV000789511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ser112Arg
CA398739800
NM_001281456.2:c.336T>G
CA398739802
NM_001281456.2:c.336T>A
CA398739808
NM_001281456.2:c.334A>C