Canonical Allele Identifier: CA913178123
Gene:

Linked Data

ClinVar Variation Id: 689911
ClinVar RCV Id: RCV000850763
dbSNP Id: rs1603219456

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4429G>A , J01415.2:m.4429G>A GRCh38