Canonical Allele Identifier: CA414774329
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4166A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4166A>T , J01415.2:m.4166A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.860A>T ENSP00000354687.2:p.His287Leu
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