Canonical Allele Identifier: PA2741919767
Gene: NOG HGNC NCBI

Linked Data

ClinVar Variation Id: 2647949
ClinVar RCV Id: RCV003428344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005441.1:p.Trp205Arg
CA399966707
NM_005450.6:c.613T>A
CA399966708
NM_005450.6:c.613T>C