Canonical Allele Identifier: CA913169087

Gene:

Linked Data

• ClinVar Variation Id: 689866
• ClinVar RCV Id: RCV000850704
• dbSNP Id: rs1057516057

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3275C>G , J01415.2:m.3275C>G	GRCh38