Canonical Allele Identifier: PA658665288
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 454055
ClinVar RCV Id: RCV003231524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro1726Arg
CA362305569
NM_022455.5:c.5177C>G