Canonical Allele Identifier: PA111139
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg1984Gln
CA295010
NM_022455.5:c.5951G>A