Canonical Allele Identifier: PA2829998579
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2574909
ClinVar RCV Id: RCV003319806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg1019Gly
CA362321773
NM_022455.5:c.3055C>G