Linked Data
ClinVar Variation Id:
235705
ClinVar RCV Id:
RCV000224389
dbSNP Id:
rs878853097
MyVariant Identifiers:
chrMT:g.8818C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.8818C>T , J01415.2:m.8818C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361899.2:c.292C>T | ENSP00000354632.2:p.Leu98= |