Canonical Allele Identifier: CA414807325
Gene: MT-ND4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10880T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10880T>C , J01415.2:m.10880T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361381.2:c.121T>C ENSP00000354961.2:p.Phe41Leu
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