Canonical Allele Identifier: PA2580454636
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2421172
ClinVar RCV Id: RCV003232855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Pro2279Leu
CA362326320
NM_022455.5:c.6836C>T