Canonical Allele Identifier: CA913177897

Gene:

Linked Data

• ClinVar Variation Id: 689893
• ClinVar RCV Id: RCV000850744 ; RCV000992387
• dbSNP Id: rs1603219427

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4370T>C , J01415.2:m.4370T>C	GRCh38