Canonical Allele Identifier: PA658809352
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 512523
ClinVar RCV Id: RCV001712656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ser2263Leu
CA3578042
NM_022455.5:c.6788C>T