Canonical Allele Identifier: CA913179843
Gene:

Linked Data

ClinVar Variation Id: 689939
ClinVar RCV Id: RCV000850793
dbSNP Id: rs1603220020

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5554C>A , J01415.2:m.5554C>A GRCh38