Canonical Allele Identifier: CA414815328
Gene: MT-ND5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.12886C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12886C>T , J01415.2:m.12886C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.550C>T ENSP00000354813.2:p.Leu184Phe
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