Canonical Allele Identifier: PA110173
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8436
ClinVar RCV Id: RCV000008951 RCV000992662 RCV001047019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ala67Pro
CA340786
NM_000304.4:c.199G>C