Canonical Allele Identifier: CA913179965
Gene:

Linked Data

ClinVar Variation Id: 689951
ClinVar RCV Id: RCV000850808
dbSNP Id: rs1603220045

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5600A>G , J01415.2:m.5600A>G GRCh38