Canonical Allele Identifier: CA913169963

Gene:

Linked Data

• ClinVar Variation Id: 690184
• ClinVar RCV Id: RCV000851071
• dbSNP Id: rs1603223647

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12279A>T , J01415.2:m.12279A>T	GRCh38