Canonical Allele Identifier: CA913169581

Gene:

Linked Data

• ClinVar Variation Id: 690144
• ClinVar RCV Id: RCV000851026
• dbSNP Id: rs1556424075

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12173T>A , J01415.2:m.12173T>A	GRCh38