Canonical Allele Identifier: CA913178560
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692477
ClinVar RCV Id: RCV000853793
dbSNP Id: rs1603219551
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4676C>A , J01415.2:m.4676C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.207C>A ENSP00000355046.4:p.Ile69=
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