Canonical Allele Identifier: PA2580454632
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2073444
ClinVar RCV Id: RCV003232738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser2263Thr
CA3578041
NM_022455.5:c.6787T>A