Canonical Allele Identifier: CA913177946

Gene:

Linked Data

• ClinVar Variation Id: 689898
• ClinVar RCV Id: RCV000850749
• dbSNP Id: rs1603219434

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4381A>G , J01415.2:m.4381A>G	GRCh38