Canonical Allele Identifier: PA2741981665
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2578222
ClinVar RCV Id: RCV003325821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser1909Pro
CA362312807
NM_022455.5:c.5725T>C