Canonical Allele Identifier: PA2826184616
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_001180384.1:p.Pro725Gln
CA154170
NM_001193455.2:c.2174C>A