Allele Registry

Canonical Allele Identifier: CA337095922

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.663A>G

Linked Data - NCBI & NCI

ClinVar Allele:

793917

ClinVar RCV:

RCV000992381

ClinVar Variation:

805059

dbSNP:

56489998

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.663A>G , J01415.2:m.663A>G	GRCh38

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