Canonical Allele Identifier: PA2580454178
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497752
ClinVar RCV Id: RCV003214137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser273Pro
CA362295892
NM_022455.5:c.817T>C