Canonical Allele Identifier: PA223641
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 96034
ClinVar RCV Id: RCV000082099 RCV002313817 RCV003231117 RCV003935067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Met455Thr
CA223639
NM_022455.5:c.1364T>C