Canonical Allele Identifier: CA658682658

Gene:

Linked Data

• ClinVar Variation Id: 986458
• ClinVar RCV Id: RCV002291222
• ERepo: CA658682658/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3280A>G , J01415.2:m.3280A>G	GRCh38