Canonical Allele Identifier: PA916055009
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 8440
ClinVar RCV Id: RCV000023072 RCV002512924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Trp28Arg
CA342724
NM_153322.3:c.82T>C
CA398271198
NM_153322.3:c.82T>A