Canonical Allele Identifier: CA913169792
Gene:

Linked Data

ClinVar Variation Id: 690165
ClinVar RCV Id: RCV000851050
dbSNP Id: rs1603223627
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12231C>T , J01415.2:m.12231C>T GRCh38
Search 100 bp 5'
Search 100 bp 3'