Canonical Allele Identifier: PA2580479027
Gene: COA8 HGNC NCBI

Linked Data

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

HGVS (amino-acid) Matching Registered Transcripts
NP_115750.2:p.Ala51Thr
CA7365420
NM_032374.4:c.151G>A
CA2160367108
NM_032374.4:c.150_151delinsAA