ClinGen Allele Registry
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Canonical Allele Identifier:
CA337100091
Gene: MT-ND6
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.14560G>A
Linked Data - NCBI & NCI
dbSNP:
28357676
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14560G>A , J01415.2:m.14560G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.114C>T
ENSP00000354665.2:p.Val38=
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