Canonical Allele Identifier: PA2829998774
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304699
ClinVar RCV Id: RCV001764935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Val1154Met
CA132831469
NM_022455.5:c.3460G>A