Canonical Allele Identifier: CA414779920
Gene: MT-ND2 HGNC NCBI

Linked Data

dbSNP Id: rs1603219909
MyVariant Identifiers: chrMT:g.5343T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5343T>C , J01415.2:m.5343T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361453.3:c.874T>C ENSP00000355046.4:p.Phe292Leu
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