Canonical Allele Identifier: CA913178020
Gene:

Linked Data

ClinVar Variation Id: 689908
ClinVar RCV Id: RCV000850760
dbSNP Id: rs1603219449
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4400A>G , J01415.2:m.4400A>G GRCh38
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