Allele Registry

Canonical Allele Identifier: PA111242

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231081

ClinVar Variation:

4139

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.His2143Gln	CA281540 NM_022455.5:c.6429C>G CA362321001 NM_022455.5:c.6429C>A