Canonical Allele Identifier: PA2580454625
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755095
ClinVar RCV Id: RCV002367246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Thr2241Ile
CA362325265
NM_022455.5:c.6722C>T