Canonical Allele Identifier: CA913161279

Gene:

Linked Data

• ClinVar Variation Id: 667034
• ClinVar RCV Id: RCV000825653
• dbSNP Id: rs1603218523

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1106C>T , J01415.2:m.1106C>T	GRCh38