Linked Data
ClinVar Variation Id:
235696
ClinVar RCV Id:
RCV000224136
dbSNP Id:
rs7340086
MyVariant Identifiers:
chrMT:g.6071T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.6071T>C , J01415.2:m.6071T>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361624.2:c.168T>C | ENSP00000354499.2:p.Val56= |