Canonical Allele Identifier: CA913163112
Gene:

Linked Data

ClinVar Variation Id: 690113
ClinVar RCV Id: RCV000850993
dbSNP Id: rs1603222827

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10408T>C , J01415.2:m.10408T>C GRCh38