ClinGen Allele Registry
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Canonical Allele Identifier:
CA414774212
Gene: MT-ND1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.4114T>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.4114T>G , J01415.2:m.4114T>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361390.2:c.808T>G
ENSP00000354687.2:p.Phe270Val
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