Canonical Allele Identifier: PA2829998584
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1799304
ClinVar RCV Id: RCV002444151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg1019Pro
CA362321779
NM_022455.5:c.3056G>C