Canonical Allele Identifier: CA913175190

Gene:

Linked Data

• ClinVar Variation Id: 690232
• ClinVar RCV Id: RCV000851124
• dbSNP Id: rs1603225587

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15914A>G , J01415.2:m.15914A>G	GRCh38