Linked Data
ClinVar Variation Id:
692352
ClinVar RCV Id:
RCV000853655
dbSNP Id:
rs386828905
MyVariant Identifiers:
chrMT:g.3399A>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.3399A>T , J01415.2:m.3399A>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361390.2:c.93A>T | ENSP00000354687.2:p.Ile31= |