Canonical Allele Identifier: CA913177963
Gene:

Linked Data

ClinVar Variation Id: 689903
ClinVar RCV Id: RCV000850754
dbSNP Id: rs1569483940
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4386T>C , J01415.2:m.4386T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'