Canonical Allele Identifier: CA414819202
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.13717A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13717A>C , J01415.2:m.13717A>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1381A>C ENSP00000354813.2:p.Ser461Arg
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