Canonical Allele Identifier: CA274531
Gene:

Linked Data

ClinVar Variation Id: 162369
ClinVar RCV Id: RCV000169780 RCV002247548
dbSNP Id: rs786200950
MyVariant Identifiers: chrMT:g.5631G>A (hg38)
ERepo: CA274531/MONDO:0044970/014
PubMed: PMID:25873012
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5631G>A , J01415.2:m.5631G>A GRCh38
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