Canonical Allele Identifier: PA658665261
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449587
ClinVar RCV Id: RCV001573572 RCV002316475 RCV003231515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg1072Gln
CA3577396
NM_022455.5:c.3215G>A