Canonical Allele Identifier: CA120558
Gene:

Linked Data

ClinVar Variation Id: 9586
ClinVar RCV Id: RCV000010203 RCV000851084 RCV003153297
dbSNP Id: rs121434462
MyVariant Identifiers: chrMT:g.12315G>A (hg38)
ERepo: CA120558/MONDO:0044970/014
PubMed: PMID:8923013
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12315G>A , J01415.2:m.12315G>A GRCh38
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