Canonical Allele Identifier: PA2827063608
Gene: COX15 HGNC NCBI

Linked Data

ClinVar Variation Id: 214263
ClinVar RCV Id: RCV000195853 RCV000321049 RCV003927838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307905.1:p.Pro131Arg
CA320228
NM_001320976.2:c.392C>G