Canonical Allele Identifier: CA913179087
Gene:

Linked Data

ClinVar Variation Id: 690082
ClinVar RCV Id: RCV000850958
dbSNP Id: rs1603221421

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8358A>G , J01415.2:m.8358A>G GRCh38