Canonical Allele Identifier: CA913170150
Gene:

Linked Data

ClinVar Variation Id: 690197
ClinVar RCV Id: RCV000851086
dbSNP Id: rs1603223668
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12335T>C , J01415.2:m.12335T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'