Canonical Allele Identifier: CA913177829

Gene:

Linked Data

• ClinVar Variation Id: 689891
• ClinVar RCV Id: RCV000850741
• dbSNP Id: rs1603219419

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4353T>C , J01415.2:m.4353T>C	GRCh38