Canonical Allele Identifier: CA913179887
Gene:

Linked Data

ClinVar Variation Id: 689945
ClinVar RCV Id: RCV000850801
dbSNP Id: rs1603220030

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5567T>C , J01415.2:m.5567T>C GRCh38