Canonical Allele Identifier: CA913163099

Gene:

Linked Data

• ClinVar Variation Id: 690111
• ClinVar RCV Id: RCV000850991
• dbSNP Id: rs1603222825

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10405T>C , J01415.2:m.10405T>C	GRCh38