Canonical Allele Identifier: CA913168941

Gene:

Linked Data

• ClinVar Variation Id: 689855
• ClinVar RCV Id: RCV000850686
• dbSNP Id: rs1603218849

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3236A>G , J01415.2:m.3236A>G	GRCh38