Canonical Allele Identifier: CA913180518

Gene:

Linked Data

• ClinVar Variation Id: 2505112
• ClinVar RCV Id: RCV003233292
• dbSNP Id: rs2124593094

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5805A>G , J01415.2:m.5805A>G	GRCh38