Canonical Allele Identifier: CA913169888
Gene:
ClinVar Allele:
677569
ClinVar RCV:
RCV000851064
ClinVar Variation:
690177
dbSNP:
118203888
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12258C>T , J01415.2:m.12258C>T GRCh38
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