Canonical Allele Identifier: PA2829998643
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2414168
ClinVar RCV Id: RCV003232848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser1061Cys
CA3577392
NM_022455.5:c.3181A>T