Canonical Allele Identifier: CA913180714

Gene:

Linked Data

• ClinVar Variation Id: 690021
• ClinVar RCV Id: RCV000850880
• dbSNP Id: rs1603220160

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5867C>T , J01415.2:m.5867C>T	GRCh38