Canonical Allele Identifier: PA2826104928
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349681
ClinVar RCV Id: RCV002047108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Leu123Ser
CA371557496
NM_001172086.2:c.368T>C