ClinGen Allele Registry
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Canonical Allele Identifier:
CA414815398
Gene: MT-ND5
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.12900A>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.12900A>T , J01415.2:m.12900A>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361567.2:c.564A>T
ENSP00000354813.2:p.Ter188Cys
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