Canonical Allele Identifier: PA916055220
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 580036
ClinVar RCV Id: RCV000703465 RCV000857017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Arg159Pro
CA398739429
NM_153322.3:c.476G>C