Canonical Allele Identifier: CA120562
Gene:

Linked Data

ClinVar Variation Id: 9592
ClinVar RCV Id: RCV000850713 RCV003162234 RCV004554594
dbSNP Id: rs199474660
MyVariant Identifiers: chrMT:g.3303C>T (hg38)
ERepo: CA120562/MONDO:0044970/014
PubMed: PMID:7906985 PMID:10431114
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3303C>T , J01415.2:m.3303C>T GRCh38
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