Canonical Allele Identifier: CA913168969

Gene:

Linked Data

• ClinVar Variation Id: 1684918
• ClinVar RCV Id: RCV002248010
• dbSNP Id: rs2124591503

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3244G>A , J01415.2:m.3244G>A	GRCh38