Canonical Allele Identifier: PA223513
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 95879
ClinVar RCV Id: RCV000081927 RCV000259059 RCV000359739 RCV001079497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060399.1:p.Ala243Val
CA223512
NM_017929.6:c.728C>T