Canonical Allele Identifier: CA913180175
Gene:

Linked Data

ClinVar Variation Id: 560167
ClinVar RCV Id: RCV000757895
dbSNP Id: rs1569484022

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5667G>A , J01415.2:m.5667G>A GRCh38