Canonical Allele Identifier: PA2826104872
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1375390
ClinVar RCV Id: RCV001879645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Asn92Thr
CA371557707
NM_001172086.2:c.275A>C