Canonical Allele Identifier: PA2573190551
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Ala174Thr
CA398248702
NM_001303.4:c.520G>A