Canonical Allele Identifier: CA913180023
Gene:

Linked Data

ClinVar Variation Id: 689959
ClinVar RCV Id: RCV000850816
dbSNP Id: rs1603220060

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5618T>C , J01415.2:m.5618T>C GRCh38