ClinGen Allele Registry
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Canonical Allele Identifier:
CA414823247
Gene: MT-ND6
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.14607G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14607G>A , J01415.2:m.14607G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.67C>T
ENSP00000354665.2:p.Pro23Ser
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