Canonical Allele Identifier: CA414812329
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693407
ClinVar RCV Id: RCV000854775
dbSNP Id: rs1603223527
MyVariant Identifiers: chrMT:g.12063C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12063C>T , J01415.2:m.12063C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.1304C>T ENSP00000354961.2:p.Thr435Ile
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