Canonical Allele Identifier: CA658475592
Gene:

Linked Data

ClinVar Variation Id: 689872
ClinVar RCV Id: RCV000850714
dbSNP Id: rs1603219385
COSMIC: COSN1085330 COSN1085331 COSN1085332 COSN1085333 COSN1085334 COSN1085335 COSN1085336
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4264G>A , J01415.2:m.4264G>A GRCh38
Search 100 bp 5'
Search 100 bp 3'