Canonical Allele Identifier: PA223672
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu1130Gly
CA223670
NM_022455.5:c.3389A>G