Canonical Allele Identifier: PA2829998768
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731481
ClinVar RCV Id: RCV002457133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Leu1148Val
CA362324652
NM_022455.5:c.3442C>G