ClinGen Allele Registry
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Canonical Allele Identifier:
CA414821855
Gene: MT-ND6
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.14304A>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14304A= , J01415.2:m.14304A=
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.370T=
ENSP00000354665.2:p.Ter124=
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