Canonical Allele Identifier: CA913179872
Gene:

Linked Data

ClinVar Variation Id: 689943
ClinVar RCV Id: RCV000850799
dbSNP Id: rs1603220027

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5563G>A , J01415.2:m.5563G>A GRCh38