Canonical Allele Identifier: PA2499289264
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002374
ClinVar RCV Id: RCV003232291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Gly2209Trp
CA362324442
NM_022455.5:c.6625G>T