Canonical Allele Identifier: PA645437801
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283556
ClinVar RCV Id: RCV000333896 RCV003231432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Val1620Ile
CA3577717
NM_022455.5:c.4858G>A