Canonical Allele Identifier: PA094039
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7522
ClinVar RCV Id: RCV000007956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Asn204Lys
CA118859
NM_001303.4:c.612C>A
CA398248888
NM_001303.4:c.612C>G