Canonical Allele Identifier: CA913163341
Gene:

Linked Data

ClinVar Variation Id: 690123
ClinVar RCV Id: RCV000851003 RCV001796796
dbSNP Id: rs1603222840
ERepo: CA913163341/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10455A>G , J01415.2:m.10455A>G GRCh38
Search 100 bp 5'
Search 100 bp 3'