Linked Data
ClinVar Variation Id:
143877
ClinVar RCV Id:
RCV000133416
dbSNP Id:
rs527236174
MyVariant Identifiers:
chrMT:g.15226A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15226A>G , J01415.2:m.15226A>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361789.2:c.480A>G | ENSP00000354554.2:p.Leu160= |