Canonical Allele Identifier: PA2829998628
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040989
ClinVar RCV Id: RCV003232323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asn1041Asp
CA3577381
NM_022455.5:c.3121A>G