Allele Registry

Canonical Allele Identifier: CA254830

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.5877C>T

Linked Data - NCBI & NCI

ClinVar Allele:

24591

ClinVar RCV:

RCV000010161

ClinVar Variation:

9552

dbSNP:

118203893

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5877C>T , J01415.2:m.5877C>T	GRCh38

Search 100 bp 5'

Search 100 bp 3'