Canonical Allele Identifier: PA2826872839
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1681856
ClinVar RCV Id: RCV002236625 RCV002487034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289583.2:p.Glu29Lys
CA7365410
NM_001302654.2:c.85G>A