Canonical Allele Identifier: PA658665327
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 454058
ClinVar RCV Id: RCV000543532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gln2030Pro
CA362316494
NM_022455.5:c.6089A>C