Allele Registry

Canonical Allele Identifier: PA294997

Gene: NSD1 HGNC NCBI

ClinVar RCV:

RCV003231282

ClinVar Variation:

159383

HGVS (amino-acid)	Matching Registered Transcripts
NP_071900.2:p.Ile1962Thr	CA294995 NM_022455.5:c.5885T>C