Canonical Allele Identifier: CA414820074

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693631
• ClinVar RCV Id: RCV000855009
• dbSNP Id: rs1603224410
• MyVariant Identifiers: chrMT:g.13913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13913T>C , J01415.2:m.13913T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1577T>C	ENSP00000354813.2:p.Leu526Pro