Canonical Allele Identifier: CA913175426
Gene:

Linked Data

ClinVar Variation Id: 690272
ClinVar RCV Id: RCV000851170
dbSNP Id: rs1603225634
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16003T>C , J01415.2:m.16003T>C GRCh38
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Search 100 bp 3'