Canonical Allele Identifier: CA280144
Gene:

Linked Data

ClinVar Variation Id: 9600
ClinVar RCV Id: RCV000010223 RCV000850687
dbSNP Id: rs193303018
MyVariant Identifiers: chrMT:g.3242G>A (hg38)
PubMed: PMID:14576046 PMID:20550934
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3242G>A , J01415.2:m.3242G>A GRCh38
Search 100 bp 5'
Search 100 bp 3'