Canonical Allele Identifier: CA913180416
Gene:

Linked Data

ClinVar Variation Id: 689981
ClinVar RCV Id: RCV000850839
dbSNP Id: rs1556423031
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5772G>A , J01415.2:m.5772G>A GRCh38
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