Canonical Allele Identifier: PA2826184439
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_001180384.1:p.Val218Leu
CA3192682
NM_001193455.2:c.652G>C
CA359125338
NM_001193455.2:c.652G>T