Canonical Allele Identifier: PA2826623543
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 384327
ClinVar RCV Id: RCV000435815 RCV000687146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268384.1:p.Gly150Arg
CA16607534
NM_001281455.2:c.448G>C