Canonical Allele Identifier: CA913180158
Gene:

Linked Data

ClinVar Variation Id: 689967
ClinVar RCV Id: RCV000850824
dbSNP Id: rs1603220076

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5661A>G , J01415.2:m.5661A>G GRCh38