Canonical Allele Identifier: PA2573098448
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304199
ClinVar RCV Id: RCV001751966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579890.1:p.Ile27Ser
CA355989460
NM_133335.4:c.80T>G