Canonical Allele Identifier: CA913169846

Gene:

Linked Data

• ClinVar Variation Id: 1684925
• ClinVar RCV Id: RCV002248017
• dbSNP Id: rs28508189

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12246C>A , J01415.2:m.12246C>A	GRCh38