Canonical Allele Identifier: CA913180305
Gene:

Linked Data

ClinVar Variation Id: 689978
ClinVar RCV Id: RCV000850835
dbSNP Id: rs1603220094

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5708C>A , J01415.2:m.5708C>A GRCh38