Canonical Allele Identifier: CA913179992
Gene:

Linked Data

ClinVar Variation Id: 689958
ClinVar RCV Id: RCV000850815
dbSNP Id: rs1603220058

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5609T>C , J01415.2:m.5609T>C GRCh38