Canonical Allele Identifier: CA913178900
Gene:

Linked Data

ClinVar Variation Id: 986422
ClinVar RCV Id: RCV003153968
ERepo: CA913178900/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8306T>C , J01415.2:m.8306T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'