Canonical Allele Identifier: PA2580112151
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Val267Ala
CA4017761
NM_000288.4:c.800T>C