Allele Registry

Canonical Allele Identifier: PA295119

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231334

ClinVar Variation:

159436

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Arg2219His	CA295117 NM_022455.5:c.6656G>A