Canonical Allele Identifier: PA2829998756
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696638
ClinVar RCV Id: RCV003232569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp1146Glu
CA362324617
NM_022455.5:c.3438T>A
CA362324619
NM_022455.5:c.3438T>G