Canonical Allele Identifier: CA414806211
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10644G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10644G>T , J01415.2:m.10644G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.175G>T ENSP00000354728.1:p.Val59Leu
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