Canonical Allele Identifier: PA2573282691
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685987
ClinVar RCV Id: RCV002250154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Thr2114Arg
CA132861307
NM_022455.5:c.6341C>G