Canonical Allele Identifier: PA2829998757
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709754
ClinVar RCV Id: RCV003232590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Glu1147Gly
CA362324633
NM_022455.5:c.3440A>G