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)

Genomic Alleles

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