Canonical Allele Identifier: CA913169095
Gene:

Linked Data

ClinVar Variation Id: 689869
ClinVar RCV Id: RCV000850708
dbSNP Id: rs1603218868
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3278T>C , J01415.2:m.3278T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'