Canonical Allele Identifier: PA891851311
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 587886
ClinVar RCV Id: RCV002312372 RCV003231601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Leu2283Pro
CA3578051
NM_022455.5:c.6848T>C