Canonical Allele Identifier: PA2830071942
Gene: COA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146997
ClinVar RCV Id: RCV004442367
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115750.2:p.Met14Thr
CA391111160
NM_032374.4:c.41T>C