Canonical Allele Identifier: PA2828444657
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146997
ClinVar RCV Id: RCV004442367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357524.1:p.Met1Thr