Canonical Allele Identifier: CA658475656
Gene:

Linked Data

ClinVar Variation Id: 689942
ClinVar RCV Id: RCV000850797
dbSNP Id: rs1603220026
COSMIC: COSN1085307 COSN1085308 COSN1085309 COSN1085310 COSN1085311 COSN1085312 COSN1085313 COSN1085314 COSN1085315
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5560G>A , J01415.2:m.5560G>A GRCh38
Search 100 bp 5'
Search 100 bp 3'