Canonical Allele Identifier: CA913177714

Gene:

Linked Data

• ClinVar Variation Id: 689882
• ClinVar RCV Id: RCV000850731
• dbSNP Id: rs1603219405

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4318C>T , J01415.2:m.4318C>T	GRCh38