Canonical Allele Identifier: CA913177695

Gene:

Linked Data

• ClinVar Variation Id: 689878
• ClinVar RCV Id: RCV000850724
• dbSNP Id: rs1603219398

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4313T>C , J01415.2:m.4313T>C	GRCh38