Canonical Allele Identifier: CA337096503

Gene: MT-ND1

Linked Data

• ClinVar Variation Id: 692338
• ClinVar RCV Id: RCV000853638
• dbSNP Id: rs201969351
• MyVariant Identifiers: chrMT:g.3338T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3338T>C , J01415.2:m.3338T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361390.2:c.32T>C	ENSP00000354687.2:p.Val11Ala