Canonical Allele Identifier: PA223711
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro2526Ser
CA223709
NM_022455.5:c.7576C>T