Canonical Allele Identifier: CA337099111
Gene: MT-ND4 HGNC NCBI

Linked Data

ClinVar Variation Id: 693351
ClinVar RCV Id: RCV000854715
dbSNP Id: rs28358284
MyVariant Identifiers: chrMT:g.11177C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.11177C>T , J01415.2:m.11177C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.418C>T ENSP00000354961.2:p.Pro140Ser