Canonical Allele Identifier: PA107789
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 7790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Thr14Pro
CA119078
NM_000288.4:c.40A>C