Canonical Allele Identifier: CA913180622

Gene:

Linked Data

• ClinVar Variation Id: 690011
• ClinVar RCV Id: RCV000850869
• dbSNP Id: rs1603220148

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5839C>T , J01415.2:m.5839C>T	GRCh38