Canonical Allele Identifier: CA913168968
Gene:

Linked Data

ClinVar Variation Id: 689856
ClinVar RCV Id: RCV000850688 RCV003153872
dbSNP Id: rs199474657
ERepo: CA913168968/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3243A>T , J01415.2:m.3243A>T GRCh38
Search 100 bp 5'
Search 100 bp 3'