Canonical Allele Identifier: PA2829998611
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1727341
ClinVar RCV Id: RCV002319856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser1027Ala
CA3577372
NM_022455.5:c.3079T>G