Allele Registry

Canonical Allele Identifier: PA645437928

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV000489207

ClinVar Variation:

427023

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Leu1999Pro	CA362315984 NM_022455.5:c.5996T>C