Canonical Allele Identifier: CA913175637
Gene:

Linked Data

ClinVar Variation Id: 689819
ClinVar RCV Id: RCV000850646
dbSNP Id: rs1603218462

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.619T>C , J01415.2:m.619T>C GRCh38