Allele Registry

Canonical Allele Identifier: CA913180192

Gene:

Linked Data

ClinVar Variation Id: 689973

ClinVar RCV Id: RCV000850830 RCV001090134

dbSNP Id: rs1603220085

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5672T>C , J01415.2:m.5672T>C	GRCh38

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