Canonical Allele Identifier: CA337099357
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693390
ClinVar RCV Id: RCV000854758
dbSNP Id: rs201803948
MyVariant Identifiers: chrMT:g.11963G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11963G>A , J01415.2:m.11963G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.1204G>A ENSP00000354961.2:p.Val402Ile
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