Canonical Allele Identifier: PA658665304
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452389
ClinVar RCV Id: RCV000523134 RCV003231517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys1905Ser
CA362312687
NM_022455.5:c.5713T>A
CA362312694
NM_022455.5:c.5714G>C