Canonical Allele Identifier: PA107774
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 7781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Ala218Val
CA130482
NM_000288.4:c.653C>T