Canonical Allele Identifier: PA207717
Gene: NSUN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211761
ClinVar RCV Id: RCV000193914 RCV000281579 RCV000434232 RCV002314837 RCV003917762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060225.4:p.Arg767Gln
CA207716
NM_017755.6:c.2300G>A