Canonical Allele Identifier: PA295064
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159413
ClinVar RCV Id: RCV003231312
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp2119Gly
CA295062
NM_022455.5:c.6356A>G