Canonical Allele Identifier: PA2741981733
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637419
ClinVar RCV Id: RCV003404717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro2282Leu
CA362326399
NM_022455.5:c.6845C>T