Canonical Allele Identifier: PA294920
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159350
ClinVar RCV Id: RCV002336291 RCV003231250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser1636Phe
CA294918
NM_022455.5:c.4907C>T