Canonical Allele Identifier: CA337098800
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693282
ClinVar RCV Id: RCV000854641
dbSNP Id: rs201397417
MyVariant Identifiers: chrMT:g.10345T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10345T>C , J01415.2:m.10345T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361227.2:c.287T>C ENSP00000355206.2:p.Ile96Thr