Canonical Allele Identifier: CA913169702

Gene:

Linked Data

• ClinVar Variation Id: 690156
• ClinVar RCV Id: RCV000851041
• dbSNP Id: rs1603223614

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12204A>C , J01415.2:m.12204A>C	GRCh38