Canonical Allele Identifier: PA110428
Gene: PMP22 HGNC NCBI

Linked Data

ClinVar Variation Id: 637822
ClinVar RCV Id: RCV000790146 RCV003581730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000295.1:p.Ser79Pro
CA398268103
NM_000304.4:c.235T>C