Canonical Allele Identifier: CA337096620

Gene: MT-ND1

Linked Data

• ClinVar Variation Id: 692382
• ClinVar RCV Id: RCV000853688
• dbSNP Id: rs878991470
• MyVariant Identifiers: chrMT:g.3644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3644T>C , J01415.2:m.3644T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000361390.2:c.338T>C	ENSP00000354687.2:p.Val113Ala