Canonical Allele Identifier: PA916055048
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637834
ClinVar RCV Id: RCV000790164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Met69Arg
CA398268285
NM_153322.3:c.206T>G