Canonical Allele Identifier: PA2825119968
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 167456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000309.2:p.Ser90Phe
CA234531
NM_000318.3:c.269C>T