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Canonical Allele Identifier:
CA345761
Gene: MT-CYB
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.15670T>C
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000133458
ClinVar Variation:
143927
dbSNP:
193302997
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.15670T>C , J01415.2:m.15670T>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361789.2:c.924T>C
ENSP00000354554.2:p.His308=
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