Canonical Allele Identifier: CA414779627
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692565
ClinVar RCV Id: RCV000853882
dbSNP Id: rs1556422968
MyVariant Identifiers: chrMT:g.5277T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5277T>C , J01415.2:m.5277T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.808T>C ENSP00000355046.4:p.Phe270Leu
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