Canonical Allele Identifier: CA337098902
Gene: MT-ND4L HGNC NCBI

Linked Data

dbSNP Id: rs2853487
MyVariant Identifiers: chrMT:g.10589G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10589G>A , J01415.2:m.10589G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.120G>A ENSP00000354728.1:p.Leu40=