Canonical Allele Identifier: CA913178231
Gene:

Linked Data

ClinVar Variation Id: 689919
ClinVar RCV Id: RCV000850771
dbSNP Id: rs1603219465
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4456C>T , J01415.2:m.4456C>T GRCh38
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