Canonical Allele Identifier: CA913169043
Gene:

Linked Data

ClinVar Variation Id: 689863
ClinVar RCV Id: RCV000850700
dbSNP Id: rs1603218860
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3263C>T , J01415.2:m.3263C>T GRCh38
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