Canonical Allele Identifier: CA337096570
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 805044
ClinVar RCV Id: RCV000992359
dbSNP Id: rs28369556
MyVariant Identifiers: chrMT:g.3513C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3513C>T , J01415.2:m.3513C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.207C>T ENSP00000354687.2:p.Thr69=