Canonical Allele Identifier: CA913175400

Gene:

Linked Data

• ClinVar Variation Id: 690270
• ClinVar RCV Id: RCV000851168
• dbSNP Id: rs1603225630

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15995G>A , J01415.2:m.15995G>A	GRCh38