Canonical Allele Identifier: PA2829998752
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710620
ClinVar RCV Id: RCV002291907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Met1141Arg
CA3577433
NM_022455.5:c.3422T>G