Canonical Allele Identifier: PA916055189
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 433198
ClinVar RCV Id: RCV000499331 RCV001857035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_696997.1:p.Gly150Val
CA398739500
NM_153322.3:c.449G>T