Canonical Allele Identifier: CA913169805
Gene:

Linked Data

ClinVar Variation Id: 690167
ClinVar RCV Id: RCV000851052
dbSNP Id: rs1556424083
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12235T>C , J01415.2:m.12235T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'