Canonical Allele Identifier: CA913180677

Gene:

Linked Data

• ClinVar Variation Id: 690017
• ClinVar RCV Id: RCV000850876
• dbSNP Id: rs1603220155

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5855A>G , J01415.2:m.5855A>G	GRCh38