Canonical Allele Identifier: PA1139750889
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 950329
ClinVar RCV Id: RCV003232242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly445Arg
CA362308665
NM_022455.5:c.1333G>C