Canonical Allele Identifier: CA414774397
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4195A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4195A>T , J01415.2:m.4195A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.889A>T ENSP00000354687.2:p.Thr297Ser
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