Canonical Allele Identifier: PA645437519
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gln236His
CA3576937
NM_022455.5:c.708G>C
CA362295302
NM_022455.5:c.708G>T