Canonical Allele Identifier: PA2829998771
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1711618
ClinVar RCV Id: RCV002293134 RCV002454619 RCV003232594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn1149Thr
CA3577437
NM_022455.5:c.3446A>C