Canonical Allele Identifier: PA658669662
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 449007
ClinVar RCV Id: RCV000521510 RCV001127738 RCV002476049 RCV001127737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Pro104Leu
CA8402295
NM_001303.4:c.311C>T