Canonical Allele Identifier: PA658721140
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488392
ClinVar RCV Id: RCV003231534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.His1591Tyr
CA362354732
NM_022455.5:c.4771C>T