Canonical Allele Identifier: PA110371
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ser22Phe
CA254390
NM_000304.4:c.65C>T