Canonical Allele Identifier: CA414805808
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10552C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10552C>A , J01415.2:m.10552C>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.83C>A ENSP00000354728.1:p.Ser28Tyr