Canonical Allele Identifier: PA2580454525
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2285020
ClinVar RCV Id: RCV002858837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu1979Asp
CA362315848
NM_022455.5:c.5937A>C
CA362315849
NM_022455.5:c.5937A>T