Canonical Allele Identifier: PA2499283583
Gene: NSUN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254788
ClinVar RCV Id: RCV001658970 RCV002539624
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060225.4:p.Val253Leu
CA3192682
NM_017755.6:c.757G>C
CA359125338
NM_017755.6:c.757G>T