ClinGen Allele Registry
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Canonical Allele Identifier:
PA290465
Gene: COX10
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000124567
RCV000961080
RCV001127831
RCV001127832
RCV001802947
ClinVar Variation:
137002
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001294.2:p.Val366Leu
CA290464
NM_001303.4:c.1096G>T
CA8402532
NM_001303.4:c.1096G>C