Allele Registry

Canonical Allele Identifier: PA295091

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231324

ClinVar Variation:

159426

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.His2162Pro	CA295089 NM_022455.5:c.6485A>C