Canonical Allele Identifier: PA2741981729
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663750
ClinVar RCV Id: RCV003443466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Arg2275Lys
CA362326175
NM_022455.5:c.6824G>A