Canonical Allele Identifier: PA658817041
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 500870
ClinVar RCV Id: RCV000597196 RCV001078538 RCV004553331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Arg109Cys
CA1673278
NM_002618.4:c.325C>T