Canonical Allele Identifier: PA294873
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159325
ClinVar RCV Id: RCV002326856 RCV003231225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn1443Ser
CA294871
NM_022455.5:c.4328A>G