Allele Registry

Canonical Allele Identifier: CA254835

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.4409T>C

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000010191

ClinVar Variation:

9578

dbSNP:

118203884

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4409T>C , J01415.2:m.4409T>C	GRCh38

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