Canonical Allele Identifier: CA913171930

Gene:

Linked Data

• ClinVar Variation Id: 690209
• ClinVar RCV Id: RCV000851101
• dbSNP Id: rs1603224847

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14727T>C , J01415.2:m.14727T>C	GRCh38