Allele Registry

Canonical Allele Identifier: PA295071

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231315

ClinVar Variation:

159417

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Cys2138Tyr	CA295069 NM_022455.5:c.6413G>A