Canonical Allele Identifier: CA414805811
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10552C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.83C>T ENSP00000354728.1:p.Ser28Phe
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