Canonical Allele Identifier: PA2826105053
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404831
ClinVar RCV Id: RCV001903425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Arg193Gly
CA371557037
NM_001172086.2:c.577A>G