Canonical Allele Identifier: PA2826184623
Gene: NSUN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211761
ClinVar RCV Id: RCV000193914 RCV000281579 RCV000434232 RCV002314837 RCV003917762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180384.1:p.Arg732Gln
CA207716
NM_001193455.2:c.2195G>A