Canonical Allele Identifier: CA913171880

Gene:

Linked Data

• ClinVar Variation Id: 690207
• ClinVar RCV Id: RCV000851099 ; RCV003153876
• dbSNP Id: rs1603224840
• ERepo: CA913171880/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14710G>A , J01415.2:m.14710G>A	GRCh38