Canonical Allele Identifier: PA645437811
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.His1638Tyr
CA16618177
NM_022455.5:c.4912C>T