Canonical Allele Identifier: PA645448362
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 287432
ClinVar RCV Id: RCV000305071 RCV002487248 RCV003165752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Ala261Ser
CA8402423
NM_001303.4:c.781G>T