Allele Registry

Canonical Allele Identifier: CA913175422

Gene:

Linked Data

ClinVar Variation Id: 690271

ClinVar RCV Id: RCV000851169 RCV002249545

dbSNP Id: rs1603225633

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16002T>C , J01415.2:m.16002T>C	GRCh38

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