Canonical Allele Identifier: PA658809337
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 524707
ClinVar RCV Id: RCV003231556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys2146Tyr
CA362321047
NM_022455.5:c.6437G>A