Canonical Allele Identifier: CA414811872
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693391
ClinVar RCV Id: RCV000854759
dbSNP Id: rs1603223491
MyVariant Identifiers: chrMT:g.11964T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11964T>G , J01415.2:m.11964T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1205T>G ENSP00000354961.2:p.Val402Gly
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