Canonical Allele Identifier: PA294896
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159338
ClinVar RCV Id: RCV000340723 RCV002316941 RCV003231238 RCV003965107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Asp1522Tyr
CA294894
NM_022455.5:c.4564G>T