Canonical Allele Identifier: CA913169551
Gene:

Linked Data

ClinVar Variation Id: 690139
ClinVar RCV Id: RCV000851021
dbSNP Id: rs1603223582

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12164G>A , J01415.2:m.12164G>A GRCh38