Linked Data
ClinVar Variation Id:
143922
ClinVar RCV Id:
RCV000133453
dbSNP Id:
rs527236206
MyVariant Identifiers:
chrMT:g.15148G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15148G>A , J01415.2:m.15148G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361789.2:c.402G>A | ENSP00000354554.2:p.Pro134= |