Canonical Allele Identifier: CA913177679
Gene:

Linked Data

ClinVar Variation Id: 689875
ClinVar RCV Id: RCV000850721 RCV002291218
dbSNP Id: rs1603219396
ERepo: CA913177679/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4308G>A , J01415.2:m.4308G>A GRCh38
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