Canonical Allele Identifier: PA110203
Gene: PMP22 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Asp37Val
CA119626
NM_000304.4:c.110A>T