ClinGen Allele Registry
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Canonical Allele Identifier:
CA414812487
Gene: MT-ND4
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.12098C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.12098C>G , J01415.2:m.12098C>G
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361381.2:c.1339C>G
ENSP00000354961.2:p.Leu447Val
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