Canonical Allele Identifier: CA913169843

Gene:

Linked Data

• ClinVar Variation Id: 690171
• ClinVar RCV Id: RCV000851058
• dbSNP Id: rs1603223634

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12245T>C , J01415.2:m.12245T>C	GRCh38