Canonical Allele Identifier: PA172797
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159299
ClinVar RCV Id: RCV000146801 RCV000879987 RCV002512581 RCV003231201
ClinVar Variation Id: 1727416
ClinVar RCV Id: RCV002325756 RCV003232608 RCV003896118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Leu1030Ser
CA172795
NM_022455.5:c.3089T>C
CA2580074127
NM_022455.5:c.3089_3090delinsCT