Canonical Allele Identifier: PA2829998713
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696563
ClinVar RCV Id: RCV003324011 RCV003232568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.His1104Arg
CA3577414
NM_022455.5:c.3311A>G