Canonical Allele Identifier: CA913170000

Gene:

Linked Data

• ClinVar Variation Id: 690188
• ClinVar RCV Id: RCV000851075
• dbSNP Id: rs1603223653

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12291T>C , J01415.2:m.12291T>C	GRCh38