Canonical Allele Identifier: PA2826105049
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2176172
ClinVar RCV Id: RCV002602546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165557.2:p.Asn192Ser
CA371557042
NM_001172086.2:c.575A>G