Linked Data
ClinVar Variation Id:
446022
ClinVar RCV Id:
RCV000514156
dbSNP Id:
rs1556423587
MyVariant Identifiers:
chrMT:g.9006A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9006A>G , J01415.2:m.9006A>G | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.480A>G | ENSP00000354632.2:p.Leu160= |