Canonical Allele Identifier: CA120644
Gene: MT-ND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9721
ClinVar RCV Id: RCV000010369 RCV000144022
dbSNP Id: rs267606889
MyVariant Identifiers: chrMT:g.4681T>C (hg38)
PubMed: PMID:16738010 PMID:20301352
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4681T>C , J01415.2:m.4681T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361453.3:c.212T>C ENSP00000355046.4:p.Leu71Pro
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