Canonical Allele Identifier: PA658654418
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 445971
ClinVar RCV Id: RCV000514768 RCV000603785 RCV001122054 RCV001122055 RCV003925530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Arg431Trp
CA8402598
NM_001303.4:c.1291C>T