Canonical Allele Identifier: PA658809367
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 524687
ClinVar RCV Id: RCV003231546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ile2394Val
CA362328727
NM_022455.5:c.7180A>G