Canonical Allele Identifier: PA2580280034
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2144227
ClinVar RCV Id: RCV003068287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Pro9His
CA1673189
NM_002618.4:c.26C>A