Canonical Allele Identifier: PA2826623638
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268385.1:p.Ser72Leu
CA119620
NM_001281456.2:c.215C>T