Canonical Allele Identifier: CA913171966

Gene:

Linked Data

• ClinVar Variation Id: 690211
• ClinVar RCV Id: RCV000851103
• dbSNP Id: rs1603224850

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14739G>A , J01415.2:m.14739G>A	GRCh38