Canonical Allele Identifier: PA2825119957
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069832
ClinVar RCV Id: RCV002966667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000309.2:p.Ile83Val
CA371557773
NM_000318.3:c.247A>G