Canonical Allele Identifier: CA913178270
Gene:

Linked Data

ClinVar Variation Id: 689921
ClinVar RCV Id: RCV000850773
dbSNP Id: rs1603219467

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4466A>G , J01415.2:m.4466A>G GRCh38