Canonical Allele Identifier: CA658475697
Gene:

Linked Data

ClinVar Variation Id: 689992
ClinVar RCV Id: RCV000850850
dbSNP Id: rs1603220121
COSMIC: COSN1085297 COSN1085298 COSN1085299 COSN1085300 COSN1085301 COSN1085302 COSN1085303 COSN1085304 COSN1085305 COSN1085306
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5791G>A , J01415.2:m.5791G>A GRCh38
Search 100 bp 5'
Search 100 bp 3'