Canonical Allele Identifier: CA337095868
Gene:

Linked Data

dbSNP Id: rs41442247
MyVariant Identifiers: chrMT:g.477T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.477T>C , J01415.2:m.477T>C GRCh38
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