Canonical Allele Identifier: CA913179841
Gene:

Linked Data

ClinVar Variation Id: 689938
ClinVar RCV Id: RCV000850791
dbSNP Id: rs878853053

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5553T>G , J01415.2:m.5553T>G GRCh38