Canonical Allele Identifier: PA645485704
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 336666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Leu113Pro
CA1673282
NM_002618.4:c.338T>C