Canonical Allele Identifier: PA2829998708
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499805
ClinVar RCV Id: RCV003223897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ile1093Leu
CA362323356
NM_022455.5:c.3277A>C
CA362323361
NM_022455.5:c.3277A>T