Canonical Allele Identifier: PA2825120202
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1381225
ClinVar RCV Id: RCV001921899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000309.2:p.Thr256Ala
CA371556628
NM_000318.3:c.766A>G