Canonical Allele Identifier: CA913179811
Gene:

Linked Data

ClinVar Variation Id: 689936
ClinVar RCV Id: RCV000850789
dbSNP Id: rs1603220018

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5544T>C , J01415.2:m.5544T>C GRCh38