Canonical Allele Identifier: CA913169577

Gene:

Linked Data

• ClinVar Variation Id: 690142
• ClinVar RCV Id: RCV000851024
• dbSNP Id: rs1556424073

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12172A>G , J01415.2:m.12172A>G	GRCh38