Canonical Allele Identifier: CA913169748

Gene:

Linked Data

• ClinVar Variation Id: 690162
• ClinVar RCV Id: RCV000851047
• dbSNP Id: rs1603223621

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12218C>A , J01415.2:m.12218C>A	GRCh38