Canonical Allele Identifier: CA913163293
Gene:

Linked Data

ClinVar Variation Id: 689840
ClinVar RCV Id: RCV000850670 RCV003153871
dbSNP Id: rs1603218588
ERepo: CA913163293/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1630A>G , J01415.2:m.1630A>G GRCh38
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Search 100 bp 3'