Canonical Allele Identifier: PA2826104958
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 970378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Val135Ala
CA4788713
NM_001172086.2:c.404T>C