Allele Registry

Canonical Allele Identifier: PA294932

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231256

ClinVar Variation:

159356

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Cys1674Tyr	CA294930 NM_022455.5:c.5021G>A