Canonical Allele Identifier: CA913180555

Gene:

Linked Data

• ClinVar Variation Id: 690004
• ClinVar RCV Id: RCV000850862
• dbSNP Id: rs1603220139

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5819T>C , J01415.2:m.5819T>C	GRCh38