Canonical Allele Identifier: CA414806133
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10626T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10626T>G , J01415.2:m.10626T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.157T>G ENSP00000354728.1:p.Ser53Ala
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