ClinGen Allele Registry
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Canonical Allele Identifier:
CA414821336
Gene: MT-ND6
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.14195A>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14195A>C , J01415.2:m.14195A>C
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.479T>G
ENSP00000354665.2:p.Leu160Trp
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