Allele Registry

Canonical Allele Identifier: PA294942

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231261

ClinVar Variation:

159361

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Cys1733Tyr	CA294940 NM_022455.5:c.5198G>A