Canonical Allele Identifier: CA131012
Gene:

Linked Data

ClinVar Variation Id: 42227
ClinVar RCV Id: RCV000035052 RCV000850891
dbSNP Id: rs111033319
MyVariant Identifiers: chrMT:g.7471del (hg38)
ERepo: CA131012/MONDO:0044970/014
PubMed: PMID:7581383
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7471del , J01415.2:m.7471del GRCh38
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