Canonical Allele Identifier: PA2829998734
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2140167
ClinVar RCV Id: RCV003232784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Lys1115Arg
CA362323871
NM_022455.5:c.3344A>G