Canonical Allele Identifier: PA281550
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2202Tyr
CA281548
NM_022455.5:c.6605G>A