Canonical Allele Identifier: PA2825401085
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157196
ClinVar RCV Id: RCV003091108
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035889.1:p.Gly29Ser
CA2811813
NM_001042424.3:c.85G>A