Canonical Allele Identifier: CA913163177

Gene:

Linked Data

• ClinVar Variation Id: 690117
• ClinVar RCV Id: RCV000850997
• dbSNP Id: rs1603222829

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10420A>G , J01415.2:m.10420A>G	GRCh38