Canonical Allele Identifier: PA2825120141
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395271
ClinVar RCV Id: RCV001901135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000309.2:p.Leu210Phe
CA371556924
NM_000318.3:c.628C>T