Linked Data
ClinVar Variation Id:
235461
ClinVar RCV Id:
RCV000224556
dbSNP Id:
rs878853042
MyVariant Identifiers:
chrMT:g.9281C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.9281C>T , J01415.2:m.9281C>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362079.2:c.75C>T | ENSP00000354982.2:p.Leu25= |