Canonical Allele Identifier: CA913168996

Gene:

Linked Data

• ClinVar Variation Id: 689858
• ClinVar RCV Id: RCV000850693
• dbSNP Id: rs199474661

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3252A>T , J01415.2:m.3252A>T	GRCh38