Canonical Allele Identifier: PA294805
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159269
ClinVar RCV Id: RCV003231173 RCV001719919 RCV002312966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ala520Thr
CA294803
NM_022455.5:c.1558G>A