Canonical Allele Identifier: CA913161643
Gene:

Linked Data

ClinVar Variation Id: 690105
ClinVar RCV Id: RCV000850983
dbSNP Id: rs1603222642

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10040C>T , J01415.2:m.10040C>T GRCh38