Canonical Allele Identifier: PA658804939
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 498141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Pro29Leu
CA4017482
NM_000288.4:c.86C>T