Canonical Allele Identifier: CA913177851

Gene:

Linked Data

• ClinVar Variation Id: 689892
• ClinVar RCV Id: RCV000850742
• dbSNP Id: rs1603219422

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4360G>A , J01415.2:m.4360G>A	GRCh38