Canonical Allele Identifier: PA2826872719
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2523113
ClinVar RCV Id: RCV003265715 RCV003730494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289582.2:p.Gly31Arg
CA7365411
NM_001302653.2:c.91G>C