Canonical Allele Identifier: CA913169582

Gene:

Linked Data

• ClinVar Variation Id: 690143
• ClinVar RCV Id: RCV000851025
• dbSNP Id: rs1556424075

Genomic Alleles

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