Canonical Allele Identifier: CA913179755
Gene:

Linked Data

ClinVar Variation Id: 689926
ClinVar RCV Id: RCV000850779
dbSNP Id: rs1603220005

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5527A>G , J01415.2:m.5527A>G GRCh38