Canonical Allele Identifier: CA913170013

Gene:

Linked Data

• ClinVar Variation Id: 986494
• ClinVar RCV Id: RCV003153969
• ERepo: CA913170013/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12294G>A , J01415.2:m.12294G>A	GRCh38