Canonical Allele Identifier: PA916067219
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 800849
ClinVar RCV Id: RCV003232167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071900.2:p.Ala2009Val
CA362316175
NM_022455.5:c.6026C>T