Canonical Allele Identifier: CA913169878

Gene:

Linked Data

• ClinVar Variation Id: 690176
• ClinVar RCV Id: RCV000851063
• dbSNP Id: rs1603223640

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12255T>C , J01415.2:m.12255T>C	GRCh38