Canonical Allele Identifier: CA913180421

Gene:

Linked Data

• ClinVar Variation Id: 689983
• ClinVar RCV Id: RCV000850841
• dbSNP Id: rs1603220102

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5774T>C , J01415.2:m.5774T>C	GRCh38