Canonical Allele Identifier: PA294942
Gene: NSD1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Cys1733Tyr
CA294940
NM_022455.5:c.5198G>A