Canonical Allele Identifier: CA414819432

Gene: MT-ND5

Linked Data

• ClinVar Variation Id: 693606
• ClinVar RCV Id: RCV000854984
• dbSNP Id: rs1556424325
• MyVariant Identifiers: chrMT:g.13768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.13768T>C , J01415.2:m.13768T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361567.2:c.1432T>C	ENSP00000354813.2:p.Phe478Leu