Canonical Allele Identifier: CA913175123
Gene:

Linked Data

ClinVar Variation Id: 690212
ClinVar RCV Id: RCV000851104
dbSNP Id: rs1603225568
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15888G>A , J01415.2:m.15888G>A GRCh38
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Search 100 bp 3'