Canonical Allele Identifier: PA110351
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8432
ClinVar RCV Id: RCV000008947 RCV000494533 RCV001380437 RCV003338380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Met69Lys
CA119618
NM_000304.4:c.206T>A