Canonical Allele Identifier: CA337098884
Gene: MT-ND4L HGNC NCBI

Linked Data

dbSNP Id: rs28358280
MyVariant Identifiers: chrMT:g.10550A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10550A>G , J01415.2:m.10550A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.81A>G ENSP00000354728.1:p.Ile27Met
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