Canonical Allele Identifier: PA172791
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159290
ClinVar RCV Id: RCV000146791 RCV000557627 RCV002426704 RCV003231193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ile899Thr
CA172789
NM_022455.5:c.2696T>C