Canonical Allele Identifier: CA913170093
Gene:

Linked Data

ClinVar Variation Id: 690196
ClinVar RCV Id: RCV000851085
dbSNP Id: rs1603223664
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12318G>A , J01415.2:m.12318G>A GRCh38
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