Canonical Allele Identifier: CA913180539

Gene:

Linked Data

• ClinVar Variation Id: 690002
• ClinVar RCV Id: RCV000850860
• dbSNP Id: rs200077222

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5814T>A , J01415.2:m.5814T>A	GRCh38