Canonical Allele Identifier: CA913175148
Gene:

Linked Data

ClinVar Variation Id: 690220
ClinVar RCV Id: RCV000851112
dbSNP Id: rs1603225575

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15897G>A , J01415.2:m.15897G>A GRCh38