Canonical Allele Identifier: CA337099418
Gene:

Linked Data

ClinVar Variation Id: 440357
ClinVar RCV Id: RCV000506174 RCV000851053 RCV000992385
dbSNP Id: rs28359170
COSMIC: COSN2377961 COSN2377962 COSN2377963 COSN2377964 COSN2377965 COSN2377966 COSN2377967 COSN2377968 COSN2377969 COSN2377970 COSN2377971
MyVariant Identifiers: chrMT:g.12236G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12236G>A , J01415.2:m.12236G>A GRCh38
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