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Canonical Allele Identifier:
CA414806291
Gene: MT-ND4L
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.10664C>T
Linked Data - NCBI & NCI
dbSNP:
193302933
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.10664C>T , J01415.2:m.10664C>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361335.1:c.195C>T
ENSP00000354728.1:p.Val65=
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