Canonical Allele Identifier: PA916055148
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637835
ClinVar RCV Id: RCV000790165 RCV001873226 RCV003325975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Ser131Cys
CA398739650
NM_153322.3:c.392C>G