Canonical Allele Identifier: CA913177679

Gene:

Linked Data

• ClinVar Variation Id: 689875
• ClinVar RCV Id: RCV000850721 ; RCV002291218
• dbSNP Id: rs1603219396
• ERepo: CA913177679/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4308G>A , J01415.2:m.4308G>A	GRCh38