Canonical Allele Identifier: CA913169589

Gene:

Linked Data

• ClinVar Variation Id: 690145
• ClinVar RCV Id: RCV000851028
• dbSNP Id: rs1603223594

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12176G>A , J01415.2:m.12176G>A	GRCh38