Canonical Allele Identifier: CA913175191
Gene:

Linked Data

ClinVar Variation Id: 690233
ClinVar RCV Id: RCV000851125
dbSNP Id: rs1603225588
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15915G>A , J01415.2:m.15915G>A GRCh38
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