Canonical Allele Identifier: CA16603316
Gene:

Linked Data

ClinVar Variation Id: 377249
ClinVar RCV Id: RCV000434423
dbSNP Id: rs1057520173
MyVariant Identifiers: chrMT:g.3169C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3169C>T , J01415.2:m.3169C>T GRCh38