Canonical Allele Identifier: PA103008
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2152
ClinVar RCV Id: RCV000002234 RCV000402285 RCV000812717 RCV000780589 RCV003390634 RCV003472958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121121.1:p.Arg98Trp
CA115367
NM_001127649.3:c.292C>T