Canonical Allele Identifier: PA2826104833
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406067
ClinVar RCV Id: RCV001915647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Ile69Thr
CA371557859
NM_001172086.2:c.206T>C