Linked Data
ClinVar Variation Id:
140591
ClinVar RCV Id:
RCV000128806
dbSNP Id:
rs193302991
MyVariant Identifiers:
chrMT:g.15301G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15301G>A , J01415.2:m.15301G>A | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361789.2:c.555G>A | ENSP00000354554.2:p.Leu185= |