Canonical Allele Identifier: PA290477
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 137008
ClinVar RCV Id: RCV000124573 RCV000975987 RCV001127736 RCV001127735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Pro101Leu
CA290476
NM_001303.4:c.302C>T