Canonical Allele Identifier: CA10581200

Gene:

Linked Data

• ClinVar Variation Id: 235012
• ClinVar RCV Id: RCV000223876 ; RCV000850715 ; RCV001009555
• dbSNP Id: rs876661358
• MyVariant Identifiers: chrMT:g.4277T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4277T>C , J01415.2:m.4277T>C	GRCh38