Canonical Allele Identifier: PA111269
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211738
ClinVar RCV Id: RCV002354542 RCV003231392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Tyr1997Cys
CA319717
NM_022455.5:c.5990A>G