Canonical Allele Identifier: PA645448338
Gene: COX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 377746
ClinVar RCV Id: RCV001125643 RCV001125644 RCV001718821 RCV003950347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294.2:p.Asp31Glu
CA8402242
NM_001303.4:c.93C>A
CA398247709
NM_001303.4:c.93C>G