Canonical Allele Identifier: CA913179796
Gene:

Linked Data

ClinVar Variation Id: 689932
ClinVar RCV Id: RCV000850785
dbSNP Id: rs1603220013

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5539A>T , J01415.2:m.5539A>T GRCh38