Canonical Allele Identifier: CA414772891
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692357
ClinVar RCV Id: RCV000853661
dbSNP Id: rs1603218982
MyVariant Identifiers: chrMT:g.3488T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3488T>C , J01415.2:m.3488T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.182T>C ENSP00000354687.2:p.Leu61Pro
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