Canonical Allele Identifier: CA270779
Gene: MT-ND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 156375
ClinVar RCV Id: RCV000144458 RCV003985280
dbSNP Id: rs587780529
MyVariant Identifiers: chrMT:g.10134C>A (hg38)
PubMed: PMID:25118196
ERepo: CA270779/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10134C>A , J01415.2:m.10134C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361227.2:c.76C>A ENSP00000355206.2:p.Gln26Lys
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