Canonical Allele Identifier: PA2830071939
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2958721
ClinVar RCV Id: RCV003816944 RCV004366726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115750.2:p.Met14Val
CA7365375
NM_032374.4:c.40A>G