Canonical Allele Identifier: CA913169621

Gene:

Linked Data

• ClinVar Variation Id: 690149
• ClinVar RCV Id: RCV000851032
• dbSNP Id: rs1603223607

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12185G>A , J01415.2:m.12185G>A	GRCh38