Canonical Allele Identifier: PA154171
Gene: NSUN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129841
ClinVar RCV Id: RCV000117858 RCV000396216 RCV001668256 RCV002312199
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060225.4:p.Pro760Gln
CA154170
NM_017755.6:c.2279C>A