Canonical Allele Identifier: CA913170039
Gene:

Linked Data

ClinVar Variation Id: 690191
ClinVar RCV Id: RCV000851079
dbSNP Id: rs1603223658
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12302C>A , J01415.2:m.12302C>A GRCh38
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