Canonical Allele Identifier: PA295116
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159435
ClinVar RCV Id: RCV001753525 RCV003231333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu2214Lys
CA295114
NM_022455.5:c.6640G>A