Canonical Allele Identifier: CA913180740

Gene:

Linked Data

• ClinVar Variation Id: 690023
• ClinVar RCV Id: RCV000850882
• dbSNP Id: rs1603220163

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5876A>G , J01415.2:m.5876A>G	GRCh38