Canonical Allele Identifier: CA913169810
Gene:

Linked Data

ClinVar Variation Id: 690168
ClinVar RCV Id: RCV000851054
dbSNP Id: rs1603223632
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12237C>T , J01415.2:m.12237C>T GRCh38
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