Canonical Allele Identifier: PA175038
Gene: PEX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 162432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_722540.1:p.Leu297Pro
CA175037
NM_153818.2:c.890T>C