Canonical Allele Identifier: CA16040637
Gene:

Linked Data

ClinVar Variation Id: 370060
ClinVar RCV Id: RCV000408927 RCV000408954 RCV000662335 RCV000851097
dbSNP Id: rs1057516070
MyVariant Identifiers: chrMT:g.14706A>G (hg38)
PubMed: PMID:28027978
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14706A>G , J01415.2:m.14706A>G GRCh38
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