Canonical Allele Identifier: CA913179766
Gene:

Linked Data

ClinVar Variation Id: 689928
ClinVar RCV Id: RCV000850781
dbSNP Id: rs1603220009

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5530C>T , J01415.2:m.5530C>T GRCh38