Canonical Allele Identifier: PA645466443
Gene: COX15 HGNC NCBI

Linked Data

ClinVar Variation Id: 298412
ClinVar RCV Id: RCV000319874 RCV002520521
ClinVar Variation Id: 3069026
ClinVar RCV Id: RCV003995086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004367.2:p.Phe372Leu
CA5642037
NM_004376.7:c.1116C>G
CA378101155
NM_004376.7:c.1116C>A
CA378101160
NM_004376.7:c.1114T>C