Canonical Allele Identifier: PA149198
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96053
ClinVar RCV Id: RCV000082118 RCV003231132 RCV003915099 RCV002311707 RCV001709482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Thr1063Ala
CA149196
NM_022455.5:c.3187A>G