Canonical Allele Identifier: PA2826872559
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011681
ClinVar RCV Id: RCV001309517
ClinVar Variation Id: 1712717
ClinVar RCV Id: RCV002300889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289581.2:p.Ala38Thr
CA7365420
NM_001302652.2:c.112G>A
CA2160367108
NM_001302652.2:c.111_112delinsAA