Canonical Allele Identifier: CA913175455
Gene:

Linked Data

ClinVar Variation Id: 690274
ClinVar RCV Id: RCV000851172
dbSNP Id: rs1603225636
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16013A>G , J01415.2:m.16013A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'