Canonical Allele Identifier: CA913177698

Gene:

Linked Data

• ClinVar Variation Id: 689880
• ClinVar RCV Id: RCV000850726
• dbSNP Id: rs1603219401

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4314T>A , J01415.2:m.4314T>A	GRCh38