Canonical Allele Identifier: CA913163198
Gene:

Linked Data

ClinVar Variation Id: 1325837
ClinVar RCV Id: RCV001785374
dbSNP Id: rs2124591018
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1616A>G , J01415.2:m.1616A>G GRCh38
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