Allele Registry

Canonical Allele Identifier: PA294929

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV001753524

RCV003231255

ClinVar Variation:

159355

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Arg1663Cys	CA294927 NM_022455.5:c.4987C>T