Canonical Allele Identifier: CA337098876
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10550A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10550A>C , J01415.2:m.10550A>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.81A>C ENSP00000354728.1:p.Ile27=