Linked Data
ClinVar Variation Id:
235606
ClinVar RCV Id:
RCV000224222
dbSNP Id:
rs878853078
MyVariant Identifiers:
chrMT:g.8856G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8856G>A , J01415.2:m.8856G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.330G>A | ENSP00000354632.2:p.Ala110= |