Canonical Allele Identifier: PA891851203
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 589031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly1075Glu
CA362322919
NM_022455.5:c.3224G>A