Canonical Allele Identifier: PA111170
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg2017Trp
CA295029
NM_022455.5:c.6049C>T