Canonical Allele Identifier: PA913194806
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 618042
ClinVar RCV Id: RCV000755984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Ile127Thr
CA8402301
NM_001303.4:c.380T>C