Canonical Allele Identifier: PA2826623686
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637376
ClinVar RCV Id: RCV000789517 RCV000807479 RCV002535805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Gly107Val
CA398739843
NM_001281456.2:c.320G>T